• Search
  • Advanced Search

Search

  • HOME
  • Search
Case Report
Three Cases of female Pseudohermaphroditism with Congenital Adrenal Hyperplasia.
Yaung Sook Choi, Shin Chul Jun, Hie Ju Park, Chan Yung Kim
Clin Exp Pediatr. 1984;27(3):297-302.   Published online March 31, 1984
We have experienced three cases of female pseudohermaphroditism with congenital adrenal hyperplasia. First case was salt-losing type and the other two cases were non salt-losing type. First patient, 2 months old female infant, was admitted to hospital because of vomiting, diarrhea, dehydration and ambiguous sex. In electrolyte study, she had hyponatremia and hyperkalemia. The other two cases, 2 Years 10 Months...
A Case of Salt-losing Form of Congenital Adrenal Hyperplasia.
J H Kwon, Y A Kim, J J Kim, D H Shin
Clin Exp Pediatr. 1983;26(12):1231-1235.   Published online December 31, 1983
A" 9-month old female was admitted via emergency room in convulsive state with the chief complaints of diarrhea and vomiting. The clitoromegaly and accessory nipples on both anter- ior axillary region were noticed in her early age. Serum electrolytes revealed hyponatremia and hyperkalemia. Urinary 17-ketosteroid level and plasma renin activity were increased. After the immediate treatment of salt-losing crisis, her general condition was recovered and serum...
A Case of Female Pseudohermaphroditism With Congenital Adrenal Hyperplasia.
Hyo Jung Kim, Hye Kyung Lee, Hyang Sook Kim, Soon Jai Lee, Sung Woo Shin
Clin Exp Pediatr. 1983;26(6):589-592.   Published online June 30, 1983
We experienced a case of female pseudohermaphroditism with congenital adrenal hyperplasia. The patient, a 10 day old female infant, was presented characteristic findings such as ambiguous sex and dehydration. The vaginogram revealed normal internal genital organs. The chromosome analysis was 46, XX. The electrolyte study showed hyponatremia and hyperkalemia. The 24 hours urinary 17-ketosteroid and 17-OHCS were 2.5 mg and 0.9 mg...
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...