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20q11.2 microdeletion syndrome

ORPHA:444051Malformation syndromeNot applicableAntenatal, Neonatal

Фенотипы (19)

Облигатный (100%)2
HP:0000490Deeply set eye
HP:0001263Global developmental delay
Очень частый (80–99%)2
HP:0000348High forehead
HP:0001511Intrauterine growth retardation
Частый (30–79%)13
HP:0000316Hypertelorism
HP:0000322Short philtrum
HP:0000365Hearing impairment
HP:0000478Abnormality of the eye
HP:0000598Abnormality of the ear
HP:0000708Atypical behavior
HP:0001252Hypotonia
HP:0001884Talipes calcaneovalgus
HP:0002007Frontal bossing
HP:0002508Brainstem dysplasia
HP:0011800Midface retrusion
HP:0012385Camptodactyly
HP:0040019Finger clinodactyly
Периодический (5–29%)2
HP:0001156Brachydactyly
HP:0001181Adducted thumb

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