- Case Report
- Neurology
- Painful legs and moving toes syndrome in a 16-year-old girl
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Seung Soo Kim, Yong Seung Hwang, Young Chang Kim
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Clin Exp Pediatr. 2016;59(9):381-383. Published online September 21, 2016
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Painful legs and moving toes (PLMT) syndrome is characterized by spontaneous movements of the digits and pain in one or both lower extremities. Of the reported cases, a majority of the patients was female, and the mean age of onset was 58 years. Only one pediatric case has been reported so far. Herein, we report the first adolescent case of... |
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- A case of Becker muscular dystrophy with early manifestation of cardiomyopathy
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Ki Hyun Doo, Hye Won Ryu, Seung Soo Kim, Byung Chan Lim, Hui Hwang, Ki Joong Kim, Yong Seung Hwang, Jong-Hee Chae
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Clin Exp Pediatr. 2012;55(9):350-353. Published online September 14, 2012
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An 18-year-old boy was admitted with chest discomfort, nausea, and dyspnea at rest. At the age of 3 years, he underwent muscle biopsy and dystrophin gene analysis owing to an enlarged calf muscle and elevated serum kinase level (6,378 U/L) without overt weakness; based on the results, Becker muscular dystrophy (BMD) was diagnosed. The dystrophin gene showed deletion of exons... |
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- A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
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Jon Soo Kim, Jinyu Park, Byung-Joo Min, Sun Kyung Oh, Jin Sun Choi, Mi Jung Woo, Jong-Hee Chae, Ki Joong Kim, Yong Seung Hwang, Byung Chan Lim
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Clin Exp Pediatr. 2012;55(12):487-490. Published online December 20, 2012
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We report a case of isodicentric chromosome 15 (idic(15) chromosome), the presence of which resulted in uncontrolled seizures, including epileptic spasms, tonic seizures, and global developmental delay. A 10-month-old female infant was referred to our pediatric neurology clinic because of uncontrolled seizures and global developmental delay. She had generalized tonic-clonic seizures since 7 months of age. At referral, she could... |
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- A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation
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Se Hee Kim, Byung Chan Lim, Jong Hee Chae, Ki Joong Kim, Yong Seung Hwang
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Clin Exp Pediatr. 2010;53(6):718-721. Published online June 23, 2010
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Rubinstein-Taybi syndrome (RTS) is a congenital disorder characterized by typical facial features, broad thumbs and toes, with mental retardation. Additionally, tumors, keloids and various congenital anomalies including congenital heart defects have been reported in RTS patients. In about 50% of the patients, mutations in the CREB binding protein (CREBBP) have been found, which are understood to be associated with cell... |
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- A case of Menkes disease with unusual hepatomegaly
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Go Un Jeong, Anna Cho, Hee Hwang, Yong Seung Hwang, Ki Joong Kim, Jong Hee Chae, Jeong Kee Seo
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Clin Exp Pediatr. 2008;51(5):538-541. Published online May 15, 2008
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Menkes disease is an X-linked recessive copper transport disorder characterized by neurological deterioration, connective- tissue damage, and abnormal hair growth. It is caused by the mutation of the ATP7A gene. This report describes a four- month-old boy with neurological symptoms typical of Menkes disease plus unusual liver involvement. He developed seizures at three months of age and exhibited hypotonia, cephalhematoma,... |
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- Original Article
- Diagnostic classification and clinical aspects of floppy infants in the neonatal and pediatric intensive care units
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Eun Sun Kim, Kyung Eun Jung, Sang Duk Kim, Eo Kyung Kim, Jong Hee Chae, Han Suk Kim, June Dong Park, Ki Joong Kim, Beyong Il Kim, Yong Seung Hwang, Jung-Hwan Choi
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Clin Exp Pediatr. 2006;49(11):1158-1166. Published online November 15, 2006
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Purpose : The purpose of this study is to make a diagnostic classification and discuss a diagnostic strategy of floppy infants by investigating clinical, neurological, electrophysiological, and genetic analysis of infants admitted to intensive care units with the complaint of hypotonia.
Methods : A retrospective study was performed from Jan. 1993 to Dec. 2005 in neonatal and pediatric intensive care units... |
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- Case Report
- Three Cases of Urine Abnormalities Associated with Ketogenic Diet
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Hye Won Hahn, Ki Jung Kim, Il Soo Ha, Hae Il Jung, Yong Seung Hwang, Yong Choi
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Clin Exp Pediatr. 2001;44(6):709-713. Published online June 15, 2001
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Ketogenic diet is a high-fat, low carbohydrate, low protein diet used in treatment of pediatric epilepsy since the 1920s. Currently it is used primarily to treat refractory childhood epilepsy. Few serious complications caused by ketogenic diet have been reported. Short-term complications include dehydration, hypoglycemia, vomiting, diarrhea, and refusal to eat. Long-term complications include kidney stones, recurrent infections, metabolic derangement, hypercholesterolemia,... |
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- Two Cases of Oculocerebrorenal Syndrome of Lowe
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So Won Kim, Young Suk Yu, In-One Kim, Hae Il Cheong, Yong Seung Hwang, Yong Choi
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Clin Exp Pediatr. 1999;42(3):419-423. Published online March 15, 1999
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Oculocerebrorenal syndrome of Lowe(OCRL) is a rare X-linked disorder characterized by congenital cataract(oculo-), hypotonia, developmental delay, cognitive impairment(cerebro-), renal tubular dysfunction(renal), and growth retardation. Recently, the defective gene, OCRL-1 gene encoding [PtdIns(4,5)P2] 5-phosphatase, was cloned with mutations identified in patients. Although there have been about 200 cases of OCRL reported in English literature, only three reports have been published in... |
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- Seizure Types and EEG Findings of Juvenile Onset Idiopathic Generalized Epilepsy
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Hyunmi Kim, Won Seop Kim, Jong Shin Kim, Kangho Cho, Ki Joong Kim, Yong Seung Hwang
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Clin Exp Pediatr. 1997;40(7):991-998. Published online July 15, 1997
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Purpose : Juvenile myoclonic epilepsy, juvenile absence epilepsy, and epilepsy wth
generalized tonic clonic seizure(GTCS) on awakening are the three syndromes of idiopathic
generalized epilepsy of adolescent onset currently included in the classification of epilepsy
syndromes of the International League Against Epilepsy(ILAE). Although they differ in their
predominant seizure types, the syndromes share several seizure types. Also, there are no
unique electrophysiologic or genetic markers.... |
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- Clinical Study of Symptoms and Various Anomalies of Patients with Joubert Syndrome
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Hang Bo Jeong, Se Hee Hwang, Ki Joong Kim, Yong Seung Hwang, Seung Cheol Kim, In-One Kim
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Clin Exp Pediatr. 1997;40(3):385-392. Published online March 15, 1997
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Purpose : Joubert syndrome is known tobean autosomal recessive disorder characterized
by cerebellar vermian dysgenesis with many symptoms and variety of other
malformations. We studied the relevant symptoms and various malformations of seven
patients diagnosed as Joubert syndrome at our institution.
Methods : Seven children with cerebellarvermian dysgenesis consistent with Joubert
syndrome were included in ourstudy. Each child was diagnosed at the Seoul National
University Children's... |
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- Clinical Characteristics of Childhood Cerebrovascular Disease and Analysis on the Prognostic Factors
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Yong Seung Hwang, Moon Sun Yang
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Clin Exp Pediatr. 1995;38(3):353-365. Published online March 15, 1995
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Purpose : Cerebrovascular disease in children is more common than was once recognized and the etiology and prognosis of the disease in children are quite different from those of adults. Recently according to medical reports and clinical experiences, the incidence of childhood cerebrovascular disease is increasing in Korea.
To clarify the clinical features of childhood cerebrovascular disease and to analyze its... |
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- Neurologic Complications after Open-Heart Surgery in Children
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Tae Sung Ko, Ki Joong Kim, Dong Wook Kim, Yong Seung Hwang, Yong Jin Kim, Joon Ryang Rho
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Clin Exp Pediatr. 1993;36(9):1245-1257. Published online September 15, 1993
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Neurologic complications after open-heart surgery are not only relatively common but also often fatal. In order to know the clinical characteristics and carsative risk factors, we carried out the retrospective study on 655 patients who had been admitted and undergone OHS at Seoul National University Children's Hospital during 2-year period from July 1990 to June 1992. The results... |
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- The Effectf Zonisamide in Children with Refractory Epilepsies
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Ki Joong Kim, Soo Ahn Chae, Tae Sung Ko, Dong Wook Kim, Yong Seung Hwang
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Clin Exp Pediatr. 1993;36(8):1139-1145. Published online August 15, 1993
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Zonisamide was amministered to 20 patients with refractory epileptic seizures. The mean duration of the administration was 6 months, and the mean dosage was 7.2mg/kg/day. The efficacy of zonisamide was rated remarkable in 15% of the cases, improvement in 40%, and no change in 45%.
The response rates of zonisamide were 62.5% for myoclonic seizures, 50% for tonic-clonic seizures, 80% for... |
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- Case Report
- A Case of Unialteral Megalencephaly
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Woo Seok Kim, Nam Soo Park, Moo Young Song, Un Jun Hyoung, Jin Oh Lee, Yong Seung Hwang
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Clin Exp Pediatr. 1993;36(6):877-881. Published online June 15, 1993
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The unilateral megalencephaly is a rare brain malfromation characterized by cerebral asymmetry and cortical dysplasia caused by faulty migration of the subependymal neuroblasts.
We experienced a case of unilateral megalencephaly in a two day-old male with the chief complaint of asymmetric head appearance. Large left hemisphere with agyria, pachygyria. dilatation of lateral ventricle, and the thick cortex of the ipsilteral hemisphere... |
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- Original Article
- A Clinical Study on Duchenne Muscular Dystrophy
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Moon Sun Yang, Su Ahn Chae, Ki Joong Kim, Yong Seung Hwang
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Clin Exp Pediatr. 1992;35(5):652-658. Published online May 15, 1992
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Twenty-five cases of Duchenne muscular dystrophy(DMD) who were diagnosed in the department of pediatrics, Seoul national university hospital (from Jan. 1985 to June 1991) were reviewed. The results were as follows.
1) All of the patients were male.
2) The onset of symptoms was between two and eight years of age. The peak incidence was at four years of age.
3) Chief complaints... |
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- A Clinical Study on Infantile Spasms with ACTH Therapy
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Se Hee Hwang, Yong Seung Hwang
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Clin Exp Pediatr. 1992;35(4):459-469. Published online April 15, 1992
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Infantile spasms is a disease, causes or treatments of which are not clearly delineated. Pri-mary objectives of treatment are complete control of seizure attack and prevention of further brain damage. Forty-one patients were managed with ACTH, who were diagnosed as infantile spasms and admitted to the Department of Pediatrics, Seoul National University Hospital from July 1985 till June 1990.
The results... |
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- Case Report
- A Case of Leigh's Disease
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Il Jung Joo, Hyun Cheol Hwang, Sang Woo Kim, Yong Seung Hwang
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Clin Exp Pediatr. 1992;35(2):234-239. Published online February 15, 1992
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We experienced a case of Leigh's disease (subacute necrotizing encephalomyelopathy) in a 3-year old boy who was presented with hypertension and showed progressive respiratory arrest after giving chloral hydrate or ketamine. Almost all diagnostic tests including brain CT showed normal findings. The diagnosis could be made by MRI and TFCA (Transfemoral carotid angiography). A review of literature was also made... |
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- Original Article
- Clinical Study on Spinal Muscular Atrophies
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Soo Ahn Chae, Yong Seung Hwang
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Clin Exp Pediatr. 1992;35(12):1728-1736. Published online December 15, 1992
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Spinal muscular atrophies (SMA) are degenerative diseases of motor neurons that begin in fetal life and continue to be progressive in infancy and childhood. Since Werdnig's description of Type 1 SMA in 1891, numerous clinical and experimental studies have been carried out in America and Europe. Few cases were reported about these diseases in Korea but there was no systemic... |
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- Case Report
- Three Cases of Listeria Infection in the Immunocompromised Children
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Mee Ran Kim, Bo Young Yun, Hye Young Kang, Sung Hee Jang, Hoan Jong Lee, Yong Seung Hwang, Eui Chong Kim
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Clin Exp Pediatr. 1992;35(10):1419-1426. Published online October 15, 1992
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Infection by Listeria monocytogenes, an uncommon pathogen in immunocompromised host, has been reported in neonates, pregnant women and adults with defective cell mediated immunity but not in children in Korea. It can cause sepsis, meningitis, abortion, premature labor, intrauterine fetal infection. etc. We have experienced L. monocytogenes sepsis and/or meningitis in three children under immunosuppresive therapy for lymphoma-leukemia, cytophagic histiocytic... |
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- Original Article
- Clinical observation on tuberous sclerosis.
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Yong Seung Hwang, Yong Soo Yun
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Clin Exp Pediatr. 1991;34(7):992-998. Published online July 31, 1991
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Thirty one cases of tuberous sclerosis were seen at the Dept, of Pediatrics, Seoul National
University Children’s Hospital.
Thirteen cases (41.9%) were diagnosed before 1 year of age and the sex ratio was 2.9:1 with male
prefonderance
The clinical epileptic manifestations were seen in 28 patients (90.3%), of whom generalized tonic
clonic seizures were associated in 12 cases (42.8%) and infantile spasm in 9 cases... |
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- Observation on neurocysticercosis in childhood.
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Hae Jung Park, Seong Hee Jang, Se Hee Hwang, Jae Il Sohn, Yong Seung Hwang, Kyu Chang Wang, Byug Kyu Cho, In One Kim, Kyung Mo Yeun, Je Geun Chi, Seung Yull Cho
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Clin Exp Pediatr. 1991;34(6):877-889. Published online June 30, 1991
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A clinical study was performed on 5 patients of neurocysticercosis in childhood who admitted to the Seoul
National University Hospital for the last two years. The conclusions were as follows:
1) Boys were more than girls with the ratio of 4:1. The average age was 9.5.
2) Three out of five lived in Jeju Island. Three had familial history of taeniasis.
3) Three out of five were... |
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- Clinical observation on brainstem glioma in childhood.
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Hyun Jun Cho, Se Hee Hwang, Yong Seung Hwang, In Won Kim
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Clin Exp Pediatr. 1991;34(4):532-543. Published online April 30, 1991
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We studied 20 cases with brainstem glioma in childhood who admitted to the Department of
Pediatrics and Pediatric Neurosurgery from Oct. 1985 till July 1990.
The results were as follows:
1) About 13.5% of all pediatric brain tumors were brainstem gliomas. The mean age on diagnosis
was 7.2 years and there was no difference in sex about the incidence and age distribution.
2) The symptom duration until... |
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- The incidence of complications in severely obese children.
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Dong Hwan Lee, Chong Guk Lee, Chul Lee, Yong Seung Hwang, Sung Ho Cha, Yong Choi
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Clin Exp Pediatr. 1991;34(4):445-453. Published online April 30, 1991
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The measurement of body weight, height and blood pressure, urine sugar, oral glucose tolerance
test, S-GOT, S-GPT, cholesterol, triglyceride, HDL-cholesterol, LDL-cholesterol tests were made
in 324 severely obese elementary, middle and high school students (218 boys and 106 girls) to know the
incidence of complication in these children. .
The results were as follow:
1) S-GOT or S-GPT were increased abnormally in 38.3% and fatty livers were... |
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- Clinical Observation of Encephalitis Empasizing the Clinically Suspected Herpes Encephalitis Cases.
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Young Sook Lee, Young Don Lee, Yong Seung Hwang
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Clin Exp Pediatr. 1990;33(5):615-622. Published online May 31, 1990
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The prognosis in all encephalitis is guarded with respect to both immediate outcome and sequelae.
But, in fact, there is no specific treatment agent for encephatitis except herpes encephalitis which is
almost fatal without adequate treatment. Acyclovir(9- [2-hydroxyethoxymetry] -guanine) has proved
to be a safe and effective agent for therapy of early stage of herpes simplex virus infections. So, in
herpes encephalitis, early diagnosis... |
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- Clinical Observation on Moyamoya Disease in Childhood.
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Se Hee Hwang, Jae Il Sohn, Yong Seung Hwang
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Clin Exp Pediatr. 1990;33(2):178-188. Published online February 28, 1990
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Although the etiology and treatment of moyamoya disease are unknown, the surgical correction is
expected as a good treatment method. But its effectiveness is not confirmed until now. A clinical
study was performed on 21 patients of moyamoya disease in childhood who admitted to the
Pediatric and Neurosurgical department of SNUCH from Jan. 1980 till July 1989.
The results were as follows:
1) The ratio of... |
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- A Case of MELAS Syndrome.
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Ki Joong Kim, Yong Seung Hwang, Young In Choi, Sung Hye Park, Je Geun Chi
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Clin Exp Pediatr. 1990;33(11):1586-1592. Published online November 30, 1990
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MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode)
syndrome is a rare but clinicopathologically distinctive mitochondrial disorder. We experienced a
case of MELAS syndrnmp in A 11 year-old girl who showed repeated attacks of stroke-like episodes,
vomitng, cortical blindness, hearing deficit and alternating hemiplegia. Serum lactic acid level was
elevated (6.4 mmol/Z). The diagnosis was confirmed by muscle biopsy which revealed dispersed
ragged-red fibers. |
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- Cardiac Tumor in Children.
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Eun Jung Bae, Young Hwue Kim, Jung Yun Choi, Yong Seung Hwang, Hyo Seop Ahn, Yong Soo Yun
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Clin Exp Pediatr. 1990;33(11):1540-1547. Published online November 30, 1990
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Primary cardiac tumor is very rare and has been a medical curiosity but is potentially curable by
current management with improvements of the imaging apparatus and the surgical technique.
Metastatic cardiac tumor is also very rare and is more difficult to diagnose than primary ones
because of lack of specific symptoms.
Twelve cases of cardiac tumor, collected from 1978 to 1989 at the Department... |
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- A Clinical Study of Periventricular-Intraventricular Hemorrhage in Very Low Birth Weight Infants.
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Myoung Jae Chey, Young Pyo Chang, Jung Hwan Choi, Yong Seung Hwang, Chong Ku Yun, In One Kim, Kyung Mo Yeon
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Clin Exp Pediatr. 1990;33(10):1341-1352. Published online October 31, 1990
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34 very low birth weight infants weighing 1,500 gms or less, who were admitted to the neonatal
intensive care unit of Seoul National University Children’s Hospital, were routinely studied with
serial real-time brain ultrasonography from August 1, 1986 to July 31, 1988.
Their medical records and the results of brain ultrasonography were analyzed to evaluate propor-
tion, severity, timing, clinical findings, outcome, associated periventricular... |
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- Late Infantile Metachromatic Leukodystrophy-Arylsulfatase A Assay in 24h Urine.
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Hong Jin Lee, Yong Joon Shin, Yong Seung Hwang, Hyung Ro Moon, Jeong Seon Seo
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Clin Exp Pediatr. 1989;32(7):978-983. Published online July 31, 1989
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A 2 year 5 month old female infant with late infantile metachromatic leukodystrophy was
diagnosed by typical clinical and laboratory findings and Arylsulfatase A assay in 24h urine. The
patient’s mother was confirmed as a heterozygote by Arylsulfatase A activities in 24h urine which
was about one half of normal control groups. |
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- Clinical Observation on Guillain-Barre Syndrome in Children.
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Byung Ran Yun, Hye Kyung Han, Yong Seung Hwang
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Clin Exp Pediatr. 1989;32(1):52-61. Published online January 31, 1989
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Clinical observation was performed on 65 cases of Guillain -Barré syndrome which were en at the
Department of Pediatrics, Seoul National University Hospital, during the past 10 years from January
1977 to December 1986.
The results were as follows:
1) The ratio of male to female was 2:1 and 56.9% of the total cases were seen between the ages of
1-5 years.
2) The highest seasonal... |
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- Serum C-Reactive Protein in Differential Diagnosis of Meningitis in Children.
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Hae Lim Chung, Hoan Jong Lee, Yong Seung Hwang
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Clin Exp Pediatr. 1988;31(12):1588-1593. Published online December 31, 1988
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CSF findings such as cell count, differential count, protein, glucose and serum CRP determined by
capillary precipitin method evaluated in 90 patients of meningitis admitted to the pediatric ward of
Seoul National University Children’s Hospital, in terms of differential diagnosis of meningitis.
The results are as follows;
1) There was considerable overlap of CSF findings and hematQlogic values between bacterial,
aseptic and tuberculous meningitis groups.
2) All 9... |
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- Case Report
- Two Case of Infantile Cortical Hyperostosis.
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Hae Lim Chung, Heon Seok Han, Young Yull Koh, Yong Seung Hwang, kyung Mo Yeon
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Clin Exp Pediatr. 1986;29(4):441-445. Published online April 30, 1986
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We experienced 2 cases of Infantile Cortical Hyperostosis. Case I was 2V2 month old male who complained of irritability and tender swelling on extremities. Case I was 3 month old male who complained of deformities in both legs and irritability on handling above lesions. The diagnosis was established by typical clinical findings and radiological evidence A brief review of... |
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- Original Article
- A Clinical Observation of Childhood Dermatomyositis.
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Dug Ha Kim, Young Yull Koh, Yong Seung Hwang
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Clin Exp Pediatr. 1986;29(4):401-410. Published online April 30, 1986
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A clinical observation has been made on 10 cases of dermatomyositis who were admitted to the Department of Pediatrics, Seoul National University Hospital from January 1980 through December 1985.
The results are as follows; 1) The ratio of female to male cases was 2.3 : 1, and the age at onset varied from 4 years of age to 14 years of... |
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- A Clinical Study on Duchenne Muscular Dystrophy in Childhood.
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Chung Il Noh, Yong Seung Hwang
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Clin Exp Pediatr. 1985;28(6):581-586. Published online June 30, 1985
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Twenty-six cases of Duchenne muscular dystrophy (DMD) who were diagnosed in the Department of Pediatrics, Seoul National University Hospital from Jan. 1976 till Jan. 1985 were reviewed. The onset of symptoms was between two and eleven years of age. The peak incidence was at 3 years of age. Both extremities were involved in 14 cases. The degree of involvement was... |
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- A Clinical Study on Neonatal seizures.
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Chong Young Park, Myung Kul Yun, Jung Hwan Choi, Yong Seung Hwang, Chong Ku Yun
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Clin Exp Pediatr. 1985;28(3):225-235. Published online March 31, 1985
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Clinical Observations were made on 96 cases of neonatal seizure who were admitted to the Department of Pediatrics, Seoul National University Hospital during the period of 5 years from June, 1979 to May, 1984.
The results were as follows: 1)The most frequent cause of neonatal seizure was sepsis with or without meningitis
(27.4%), and followed by hypocalcemia(23.4%)> hypoxic-ischemic brain damage(12.9%), hypoglycemia(8.0%), intracranial... |
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- A clinical study on Myasthenia gravis in childhood.
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Yong Seung Hwang, Hyo Seop Ahn, Sang Hyup Kim
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Clin Exp Pediatr. 1985;28(2):154-159. Published online February 28, 1985
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Twenty-six cases of myasthenia gravis (MG) in childhood who were diagnosed and treated in the Department of Pediatrics, Seoul National University Hospital from January 1976 till October 1984 were reviewed clinically. Mean age of onset of MG was 5.4+3.6 years of age with the peak incidence at 2 years of age. Sexual difference was negligible as male to female ratio... |
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- Case Report
- A Case Report of Syringomyelia.
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Myung Kul Yum, Hye Sun Lee, Hee Sang Yoon, Yong Seung Hwang, Hyun Jip Kim
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Clin Exp Pediatr. 1985;28(1):95-98. Published online January 31, 1985
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We reported a case of syringomyelia in a 9 year old boy. His major problem was left side hemiparesis and sensory loss. Diagnosis was made by myelography and spinal CT with the use of metrizamide, and was confirmed by surgical exploration. The hemiparesis and sensory loss improved after lamincetomy and decompression.
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- Moyamoya Disease with Intraventricular Hemorrhage in a Child.
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Byoung Hai Ahn, Chung Il Noh, Yong Seung Hwang, Young Soo Yoon
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Clin Exp Pediatr. 1983;26(12):1247-1253. Published online December 31, 1983
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A 9-year-old female patient with evidence of intraventricular hemorrhage by computed
tomography was subsequently proven to have moyamoya disease by cerebral angiography.
Subarachnoid hemorrhage is the most common initial manifestation of moyamoya disease in
the adult. However, such presentation seldom occurs in childhood moyamoya disease, and
intraventricular hemorrhage has been quite rare in children. The rarity of this manifestation
of moyamoya disease and its cause... |
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- Original Article
- Statistical Analyses of the Diseases of the Nervous system: With Special Reference to the Annual Change of the Incidence.
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Yong Seung hwang, Yong Choi, Dwang Wook Ko
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Clin Exp Pediatr. 1980;23(1):41-56. Published online January 15, 1980
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Primary disorders of the nervous system admitted to the Pediatric ward of Seoul National University Hospital during 10 years from January 1969 till December 1978 were analysed to observe particularly the annual change of the incidence. Total number of the diseases of the nervous system was 1522, about 20.2% of the total admitted patients during this period. Annual incidence of... |
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- Studies on the Growth and Nutritional Status of School Children in Korean Rural Area.
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Yong Seung Hwang
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Clin Exp Pediatr. 1978;21(1):12-18. Published online January 31, 1978
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Measurements of the left mid-arm circumference, triceps skin-fold thickness, hematocrit and plasma total protein were performed in 1,084 healthy school children of Korean rural area. Comparing these data with that of school and normal Korean children, and obtaining the incidence of anemic children, nutritional status of school children in Korean rural area were evaluated. 1. Mean values of the mid-arm... |
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- Clinical Review of Tuberculous Meningitis in Children.
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Yong Seung Hwang, Chong Koo Yun, Kwang Wook Ko
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Clin Exp Pediatr. 1977;20(1):13-19. Published online January 31, 1977
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The following results were obtained through the clinical review of 89 cases of tuberculous meningitis which were treated at the Department of Pediatrics of Seoul National University Hospital during the period of 3 years from June 1973 till May. 1976. 1. The highest incidence by age was noted as 80.9% under the age of 6years and 24.7% of cases were... |
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