Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/82760
Title: Congenital adrenal hyperplasia: experience at intersex clinic, AIIMS.
Authors: Menon, P S
Virmani, A
Sethi, A K
Verma, I C
Rohatgi, M
Gupta, D K
Gupta, A K
Issue Date: 1-Jul-1992
Citation: Menon PS, Virmani A, Sethi AK, Verma IC, Rohatgi M, Gupta DK, Gupta AK. Congenital adrenal hyperplasia: experience at intersex clinic, AIIMS. Indian Journal of Pediatrics. 1992 Jul-Aug; 59(4): 531-5
Abstract: During 1981-88, 63 cases of female pseudohermaphroditism (FPH) were seen at the Intersex clinic at AIIMS, of whom 34 (54%) were diagnosed as due to congenital adrenal hyperplasia (CAH). Though ambiguity was present at birth in most cases, only one child was brought immediately after birth, while 14 presented after one year. Family history of affected siblings and fetal wastage was present in 10. Salt wasting symptoms were present in 13 (38.2%), evidence of early virilization in 10 (29.4%) and generalised hyperpigmentation in 7 (20.6%). Clitoromegaly was present in 30 children with labial fusion in 10 and scrotalisation of labia in 6. The urogenital opening was single in 25 (73.5%). Buccal smear was positive for sex chromatin in 19. Chromosomal pattern showed 46 XX in 33. Dyselectrolytemia was present in 16 children. Bone age was advanced in all. Adrenal hyperplasia could be documented in 3 on CT scan. All the girls were put on hydrocortisone or prednisolone, and fluodrocortisone was given only to children with salt wasting CAH. Children with CAH are being brought to medical attention much too late and investigative and therapeutic facilities are grossly inadequate. There is a need to educate primary care physicians for early case detection and provide minimum diagnostic and therapeutic facilities in regional centres.
URI: http://imsear.hellis.org/handle/123456789/82760
Appears in Collections:Indian Journal of Pediatrics

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