Volume : IX, Issue : VIII, August - 2019

Complete Androgen Insensitivity Syndrome: Report of a Case with Focal Segmental Glomerulosclerosis

Dr. Arshad Saleem, Dr Radha Rani, Dr P Sreenivasulu

Abstract :

Complete Androgen Insensitivity Syndrome, commonly known as the Testicular Feminization Syndrome, is characterized by a 46, XY karyotype, bilateral testes, absent or hypoplastic Wolffian ducts, and female–appeå external genitalia with diminished axillary and pubic hair development. Although initial diagnosis in the child is difficult, the syndrome must be suspected after puberty if primary amenorrhea is present. Coexistence of genital defects with urologic abnormalities is expected in these cases because of close emyologic origin. However, renal involvement in form of Nephrotic Syndrome does not seem so common. We report a case of testicular feminization syndrome with Focal Segmental Glomerulo Sclerosis.

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Article: Download PDF   DOI : 10.36106/ijar  

Cite This Article:

COMPLETE ANDROGEN INSENSITIVITY SYNDROME: REPORT OF A CASE WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS, Dr.Arshad Saleem, Dr Radha Rani, Dr P Sreenivasulu INDIAN JOURNAL OF APPLIED RESEARCH : Volume-9 | Issue-8 | August-2019

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