American Journal of Medical Genetics · 1985 · 42 citations · 12 references
MedicineEndocrinologyGeneticsHuman GeneticsPediatric EndocrinologyReproductive EndocrinologyCongenital Endocrine DisordersCongenital Reproductive AnomaliesDisorders Of Sex DevelopmentGenetic DisordersGonadal DisordersMendelian DisordersAutosomal Recessive InheritanceCongenital Mullerian AnomaliesDisorders Of Sexual DifferentiationGenetic Basis Of AlopeciaGenitalia MorphologyGonadal AplasiaInternal GenitaliaPrimary Hypogonadism
We describe 3 sibs, two females and a male, with hypogonadism, defective Müllerian development in the sisters, and partial alopecia consisting of cranial hair only in the center of the scalp. One sister had absent gonads, the other had streak ovaries; both had markedly hypoplastic internal genitalia. Their brother had hormonal and histologic findings consistent with germinal cell aplasia. In view of the fact that the parents were consanguineous, autosomal recessive inheritance of the syndrome is likely.
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A familial syndrome of deafness, alopecia, and hypogonadism
Barbara F. Crandall, Lawrence Samec, Robert S. Sparkes et al. · The Journal of Pediatrics · 1973 · 73 citations
Medicine, Endocrinology, Genetics +12
The XY Gonadal Agenesis Syndrome
Gloria E. Sarto, John M. Opitz · Journal of Medical Genetics · 1973 · 69 citations · Full text