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Case Report
A Case of Fetal Alcohol Syndrome with Persistent Pulmonary Hypertension of the Newborn
Jin-Ha Chang, Ran Namgung, Min-Soo Park, Kook In Park, Jin-Sung Lee, Chul Lee
Clin Exp Pediatr. 2004;47(11):1220-1224.   Published online November 15, 2004
Fetal alcohol syndrome can be suspected in infants born to mothers with a prenatal history of alcohol abuse if the child exhibits characteristic facial features, together with intrauterine growth retardation, multiple neurological abnormalities, and multiorgan defects. If only a few of the above criteria are satisfied, the term fetal alcohol effects is used. We experienced a neonate who presented with...
A Case of Cloacal Deformity
Young Mi Jee, Seung Jin Lee, In Kyung Sung, Byung Churl Lee
Clin Exp Pediatr. 1992;35(5):667-670.   Published online May 15, 1992
We experienced a case of cloacal deformity. This one day-old female neonate had hydrometrocolpos with vaginal atresia, imperforated anus, cloaca associated with hemivertebrae, left renal agenesis and right hydronephrosis. A brief review of related literature was made.
A Case of Unilateral Renal Agenesis Associated with Acute Renal Failure.
M J Kim, S Y Chung, H S Kim, S H Kim, C M Kang
Clin Exp Pediatr. 1986;29(11):1245-1250.   Published online November 30, 1986
The authors experienced a case of unilateral renal agenesis associated with hydronephrosis resulted from U.P.J. obstruction of contralateral kidney. The patient was a 7 year old girl who was hospitalized with sudden onset of renal failure and the diagnosis was made by intravenous pyelography, abdominal ultrasonogram and C-T scan. Patient was almost completely recovered with peritoneal dialysis and surgical operation. A brief review...
A Case of Congenital Adrenal Agenesis.
Kyeong Wha Lee, Hyung Jin Choi, Sang Man Shin, Sang Jhoo Lee, Dong Wha Lee
Clin Exp Pediatr. 1984;27(11):1118-1122.   Published online November 30, 1984
Congenital adrenal agenesis or hypoplasia is very rare disorder which causes adrenal insufficiency. It is usually the result of an isolated defect of organogenesis. It may be sporadic, or it may express itself as an autosomal recessive or X-linked disorder within families. We experienced a baby who revealed hyperpigmentation, hypoglycemia, hyperkalemia and hyponatremia immediately after birth. Hormone study was compatible with primary adrenal insufficiency. Complete...
A Case of Potter Syndrome.
Young Mi Hong, Hae Seung Kim, Jung Gon Kim, Keun Lee
Clin Exp Pediatr. 1982;25(11):1181-1184.   Published online November 30, 1982
In 1946 Potter described a series of 20 cases in infants in whom bilateral absence of the kidneys was associated with, hypoplasia of the lung and characteristic face. The main facial features she described were increased space between the eyes, a prominent fold which arises at inner canthus and sweeps downward and laterally below the eyes, unusual flattening of the nose, excessive recession of...
A Case of Rt. Renal Agenesis Combined with Cryptorchism and Neuroblastoma.
Hee Jung Chung, Chul Lee, Pyung Kill Kim, Chang Jin Kim, Kwang Kill Lee, Yu Bok Lee, Ki Keun Oh
Clin Exp Pediatr. 1981;24(7):677-684.   Published online July 15, 1981
Congenital unilateral renal agenesis is a rare congenital anomaly. Furthermore, renal agenesis associated with neuroblastoma and cryptorchism is more rare in incidence. Recently we experieced a case of Rt. renal agenesis combined with cryptorchism and neuroblastoma. We diagnosed it with IVP and selective renal angiography and confirmed it with explolaparotomy and biopsy. We reviewed the literatures on renal agenesis, cryptorchism...