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Hypergonadotropic hypogonadism-cataract syndrome

ORPHA:2410Malformation syndromeAutosomal recessiveAdolescent

Фенотипы (13)

Облигатный (100%)2
HP:0000518Cataract
HP:0000815Hypergonadotropic hypogonadism
Очень частый (80–99%)8
HP:0000144Decreased fertility
HP:0000786Primary amenorrhea
HP:0000823Delayed puberty
HP:0000837Increased circulating gonadotropin level
HP:0000939Osteoporosis
HP:0002750Delayed skeletal maturation
HP:0008187Absence of secondary sex characteristics
HP:0008240Secondary growth hormone deficiency
Частый (30–79%)3
HP:0002757Recurrent fractures
HP:0004322Short stature
HP:0004349Reduced bone mineral density

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы