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X-linked intellectual disability, Stoll type

ORPHA:85326Malformation syndromeX-linked recessiveInfancy, Neonatal

Фенотипы (12)

Частый (30–79%)12
HP:0000272Malar flattening
HP:0000316Hypertelorism
HP:0000343Long philtrum
HP:0000349Widow's peak
HP:0000455Broad nasal tip
HP:0000463Anteverted nares
HP:0001249Intellectual disability
HP:0002003Large forehead
HP:0002007Frontal bossing
HP:0004209Clinodactyly of the 5th finger
HP:0004322Short stature
HP:0005281Hypoplastic nasal bridge

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