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Definition

An autosomal recessive disease characterized by primary amenorrhea, variable development of secondary sex characteristics, poorly developed streak ovaries, and high serum levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH).

Acronym

ODG1

Synonyms

Gonadal dysgenesis XX type
Hypergonadotropic ovarian dysgenesis autosomal recessive
Hypergonadotropic ovarian dysgenesis with normal karyotype
Hypergonadotropic ovarian failure
XXGD
XX gonadal dysgenesis

 
Disclaimer

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