A rare cause for primary amenorrhea: Sporadic perrault syndrome

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 syndrome. Perrault syndrome is a rare autosomal...

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Bibliografiske detaljer
Main Authors: Ameen, K. H. Noorul, Pinninti, Rakesh
Format: Artigo
Sprog:Inglês
Udgivet: Medknow Publications & Media Pvt Ltd 2012
Fag:
Case Report with Review of Literature
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3475920/
https://ncbi.nlm.nih.gov/pubmed/23087880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.100677
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