- Original Article
- A case of 4p- syndrome with oligomeganephronia.
-
Ri Sa Lee, Bong Sik Kong, Beyong Il Kim, Sang Kyu Park, Ho Jin Park, Soong Deok Lee, Je Geun Chi
-
Clin Exp Pediatr. 1991;34(4):558-565. Published online April 30, 1991
-
|
|
The 4p_ syndrome results from structural deficiency of chromosome 4. We experienced a patient
of 4p~ syndrome who all features of already described Wolf syndrome, i.e., prominent glabella,
hypertelorism, broad beak nose, cleft lip and palate, kyphoscoliosis, hypospadia, etc.. Postmortem
examination revealed multiple visceral anomalies, including large atrial septal defect, diaphragmatic
eventration, intestinal malrotation, ankyloglossia, and hemivertebrae. The kidneys showed a marked
simple hypoplasia weighing... |
-
-
- A clinical study on neonatal seizures.
-
Bong Sik Kong, Ri Sa Lee, Sang Kyu Park, Ho Jin Park
-
Clin Exp Pediatr. 1991;34(2):230-239. Published online February 28, 1991
-
|
|
Clinical observation were made on 57 cases of neonatal seizure who were admitted to the Depart-
ment of pediatrics, Seoul Red Cross Hospital during the period of 7 years from Jan. 1983 to Dec. 1989.
The results were as follows:
1) According to the type of delivery of neonates which showed neonatal seizure, normal vaginal
delivery were 41 cases (71.9%), C-section delivary 11 cases (19.3%)... |
-
-
|
