Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype.

doi:10.1016/j.fertnstert.2010.11.034

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Article

Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype.

Fertility and sterility - 1 Apr 2011

Bagci Gulseren, Bisgin Atil, Karauzum Sibel Berker, Trak Bilal, Luleci Guven

Abstract excerpt

OBJECTIVE: To present a familial case of Swyer syndrome. DESIGN: Case report. SETTING: Academic medical center. PATIENT(S): Two sisters with a main complaint of primary amenorrhea and another case, their mother's maternal aunt with the same history of primary amenorrhea but married with no consanguinity and no children. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): The patients were studied from clinical,...

Topics

Adolescent
Adult
Amenorrhea
Family
Female
Gonadal Dysgenesis, 46,XY
Humans
Male
Mothers
Pedigree
Phenotype
Sex
Siblings

Source

Open in PubMed

Identifiers

PMID: 21145048
DOI: 10.1016/j.fertnstert.2010.11.034

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