- Incidence of hearing loss and importance of risk factors in the neonatal intensive care unit
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Seung Hyun Kong, Jang Hee Kang, Kwang Su Hwang, Joong Pyo Kim, Hyeon Jung Lee, Hyeon Choi, Ji Sun Mok, Jung Young Kim
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Clin Exp Pediatr. 2006;49(8):845-850. Published online August 15, 2006
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Purpose : To assess the incidence of neonatal hearing loss in a neonatal intensive care unit and the relative importance of risk factors for hearing imparement in a neonatal intensive care unit which the Joint Committee on Infant Hearing(JCIH) had recommended.
Methods : One thousand, two hundred and one newborns admitted to the Good Moonhwa Intensive Care Unit from May... |
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- Investigation of Automated Neonatal Hearing Screening for Early Detection of Childhood Hearing Impairment
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Jeong Il Seo, Si Uk Yoo, Sung Hyeon Gong, Kwang Su Hwang, Hyeon Jung Lee, Joong Pyo Kim, Hyeon Choi, Bo Young Lee, Ji Sun Mok
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Clin Exp Pediatr. 2005;48(7):706-710. Published online July 15, 2005
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Purpose : Early diagnosis of congenital hearing loss through the neonatal hearing screening test minimizes language defect. This research intends to identify frequency of congenital hearing loss in infants through neonatal hearing screening test with the aim of communicating the importance of hearing test for infants.
Methods : From May 20, 2003 to May 19, 2004, infants were subjected to Automated... |
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- Case Report
- A Case of Short Arm Deletion and Long Arm Duplication at Chromosome 3
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Seung Hyun Kong, Jeong Il Seo, Jang Hui Kang, So Young Jung, Ji Sun Mok
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Clin Exp Pediatr. 2005;48(12):1389-1393. Published online December 15, 2005
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The long arm duplication of chromosome 3 was reported for the first time in 1966 by Falek et al., and Hirschhorn et al. came to identify the duplication of 3q21 qter region in 1973. In most cases of duplication 3q syndrome patients, pure duplication of 3qter is believed to be rare and is often reported accompanied with deletion of another... |
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- Chondrodysplasia Punctata(Rhizomelic Type)
Associated with Pneumothorax
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Ji Sun Mok, Hye Won Hwang, Jin Eun Kim, Dong Seok Lee, Doo Kwun Kim, Seong Min Choi
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Clin Exp Pediatr. 2001;44(8):965-970. Published online August 15, 2001
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Chondrodysplasia punctata is a rare congenital syndrome caused by a peroxisomal dysfunction. Chondrodysplasia punctata is classified into four main types-Coradi-Hunermann's type, rhizomelic type, X-linked dominant form and X-linked recessive form. A male patient with this condition was born at 39 weeks gestation, the pregnancy being complicated by polyhydroamnios, breech presentation, and anomalies of congenital limbs. At delivery, there was no... |
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- A Case of Aseptic Meningitis Following Administration of Intravenous Immunoglobulin in A Patient with
Idiopathic Thrombocytopenic Purpura
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Su Jin Kim, Ji Eun Kim, Hei Won Hwang, Ji Sun Mok, Dong Seok Lee, Doo Kwun Kim, Sung Min Choi, Woo Taek Kim
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Clin Exp Pediatr. 2001;44(7):823-826. Published online July 15, 2001
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Intravenous immunoglobulin(IVIG) has been widely used to treat idiopathic thrombocytopenic purpura in childhood. Aseptic meningitis has been reported as a rare complication of IVIG therapy. This report is on an 11 year-old boy with ITP who suffered from aseptic meningitis following the administration of IVIG. He was given 1 g/kg of IVIG for 2 days, and on the fourth day... |
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- Two Cases of Leigh Disease in Siblings
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Su Jin Kim, Ji Eun Kim, Hei Won Hwang, Ji Sun Mok, Dong Seok Lee, Doo Kwun Kim, Sung Min Choi, Woo Taek Kim
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Clin Exp Pediatr. 2001;44(6):718-722. Published online June 15, 2001
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Leigh disease is a familial and degenerative disorder characterized by focal, bilateral, and usually symmetric lesions of the both gray and white matter in the brain and the spinal cord. The clinical course is variable, but in most cases, the prognosis is poor with subacute progression leading to death within months or years of life. The pathogenesis was known as... |
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