• Search
  • Advanced Search

Search

  • HOME
  • Search
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%)...
A Case of Trichobezoar.
Ue Chong Yang, Bong Sik Kong, Sang kyu Park, Ho Jin Park, Mi Ja Shin, Seok Hwan Shin
Clin Exp Pediatr. 1989;32(5):700-704.   Published online May 31, 1989
Trichobezoar is one of the rare diseases, which usually occurs in teen.aged girl who has an emotional disturbance and history of trichophagia. We experienced a case of gastric trichobezoar in a 8 year old girl, who had colicky abdominal pain and movable epigastric mass with the history of trichophagia. Diagnosis was suspected by the history of trichophagia and movable epigastric mass and confirmed by...