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Case Report
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...
Original Article
Normal Growth in the Genitalia of Korean Male Children.
Kwang Chang Doh
Clin Exp Pediatr. 1982;25(7):674-686.   Published online July 31, 1982
An accurate evaluation of the size of the genitalia and its function is mandatory in judging abnormal growth of external genitalia from birth to adolescence as well as adulthood. This study was carried out to establish the standard values of penile and testicular sizes for normal Korean boys. Nine hundred and fifty-four Korean boys from birth to 15 years of...
Case Report
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...
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