hrp0086p2-p402 | Gonads & DSD P2 | ESPE2016

Children with 46,XY DSD: Etiology, Clinical Profile, Socio-Demographic Details and Sex of Rearing

Shabir Iram , Khurana Madan , Eunice Marumudi , Ammini Ariachery

Background: Disorders of sex development (DSD) is a group of uncommon birth defects. Androgen excess in genetic females and androgen deficiency in genetic males can result in DSD. A child with ambiguous genitalia could be a virilized female or an under-masculinized male. Presented here is the socio-demographic profile, age at diagnosis, clinic 351al profile and etiology of patients with 46,XY DSD who are on follow up at our hospital.Objective and hypothe...

hrp0086p2-p418 | Gonads & DSD P2 | ESPE2016

Phenotype, Genotype and Gender Identity in Pubertal and Post-Pubertal Patients with Androgen Insensitivity Syndrome

Shabir Iram , Khurana Madan , Joseph Angela , Eunice Marumudi , Mehta Manju , Ammini Ariachery

Background: Androgen insensitivity syndrome (AIS) is a rare disease due to end organ resistance of androgens. AIS is commonly caused by the mutations of androgen receptor (AR) gene located on chromosome Xq11-12. The mode of inheritance is hemizygous, where males get severely affected and females remain as carriers.Objective and hypotheses: Here, we describe the Phenotype–Genotype correlation and gender identity of pubertal and post pubertal...