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Xp22.3 microdeletion syndrome

ORPHA:1643Malformation syndromeNot applicableNeonatal

Фенотипы (12)

Очень частый (80–99%)3
HP:0000869Secondary amenorrhea
HP:0002916Abnormality of chromosome segregation
HP:0004322Short stature
Частый (30–79%)7
HP:0000044Hypogonadotropic hypogonadism
HP:0000144Decreased fertility
HP:0000147Polycystic ovaries
HP:0000545Myopia
HP:0007759Opacification of the corneal stroma
HP:0008056Aplasia/Hypoplasia affecting the eye
HP:0008065Aplasia/Hypoplasia of the skin
Периодический (5–29%)2
HP:0000960Sacral dimple
HP:0004397Ectopic anus

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