A rare cause for primary amenorrhoea

• Päätekijät: Kaderthambi Hajamohideen Noorul Ameen (Tekijä), Rakesh Pinninti (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Wolters Kluwer Medknow Publications, 2012-01-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

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 au...