- Case Report
- A Case of Tuberous Sclelosis with Renal Angiomyolipoma.
-
H K Park, H J Park, H J Chun, M J Shin, J S Choi
-
Clin Exp Pediatr. 1982;25(11):1170-1174. Published online November 30, 1982
-
|
|
Tuberous sclerosis is a heredofamilial disease and is a multisystem disorder affecting
primarily tissues derived from ectoderm, such as skin, eye, central and peripheral nervous
system, but also involving organs of mesodermal and endodermal origins, such as heart,
lungs, kidneys, bones and GI tract. It is characterized by classical triad of mental retard-
ation, epilepsy and angiofibroma.
We experienced a full blown case of tuberous... |
-
-
- A Case of Female Pseudohermaphroditism due to Congenital Adrenal Hyperplasia and a Case of Male Pseudohermaphroditism.
-
Y S Shin, H J Park, H J Chun, M J Shin
-
Clin Exp Pediatr. 1981;24(12):1203-1208. Published online December 15, 1981
-
|
|
Recently we experienced each of female and male pseudohermaphroditisms which were admitted with complaint of ambiguous genitalia nearly at thesame time. Case 1, 12 year 7 month old, had musculine appearance with acne, beard and mustache, broad shoulders and short hair. Her phallus was large penile shape with abundant pubic hair and vaginal opening was hidden behind the fused labioscrotal... |
-
-
- A Case of Chronic Active Hepatitis.
-
H J Park, H K Park, H J Chun, M J Shin, S C Kang
-
Clin Exp Pediatr. 1981;24(10):991-996. Published online October 15, 1981
-
|
|
Chronic active hepatitis (CAH) is defined as ongoing inflammation within the liver sustained beyond the expected time of resolution. The etiology of CAH is not completely understood, but hepatitis B infection, drugs such as oxyphenisatin, isoniazid, and alpha-methyldopa, and altered immunity are considered. The most common findings are jaundice, hepatosplenomegaly, elevated serum transaminase activities, hypergammaglobulinemia, and positive "autoimmune" serologic tests,... |
-
-
- Two cases of salt losing form of congenital adrenal hyperplasia.
-
K C Park, H J Chun, M J Shin, S C Kang
-
Clin Exp Pediatr. 1978;21(9):614-621. Published online September 30, 1978
-
|
|
We experienced 2 case of losing form of congenital adrenal hyperplasia which were regarded to be sucessfully controlled with hormonal replacement, DOCA and hydrocortisone. Case 1 was a 40 days-old male infant who had hyperpigmented phallus, scrotal rugae and nipples but whose phallus seemed to be normal in size and shape. He was admitted at the age of 40 days... |
-
-
|
