A rare cause for primary amenorrhoea

A rare cause for primary amenorrhoea

Gonadal (ovarian) dysgenesis with normal chromosomes (46, XX), XX female gonadal dysgenesis (XX-GD) is a rare genetically heterogeneous disorder. In 1951, Perrault reported the association of gonadal dysgenesis and deafness, now referred to as Perrault′s syndrome. Perrault syndrome is a rare autosom...

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Bibliographic Details
Main Authors: Kaderthambi Hajamohideen Noorul Ameen, Rakesh Pinninti
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Journal of Human Reproductive Sciences
Subjects:
Deafness
karyotype
marfanoid habitus
ovarian dysgenesis
Perrault′s syndrome
Online Access:http://www.jhrsonline.org/article.asp?issn=0974-1208;year=2012;volume=5;issue=2;spage=218;epage=220;aulast=Noorul

Internet

http://www.jhrsonline.org/article.asp?issn=0974-1208;year=2012;volume=5;issue=2;spage=218;epage=220;aulast=Noorul

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