Article

Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort

2018-09-24

Abstract excerpt

Androgen insensitivity syndromes the most frequent monogenic known cause of 46,XY DSD. Mutations of variable severity in androgen receptor gene are associated with a wide phenotypic spectrum, ranging from complete androgen insensitivity syndrome to a partial form or a mild form.

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Literature Corpus work: 15346e97-0509-5aab-adb1-aeccc3ae923a
DOI: 10.4274/jcrpe.0185

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