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Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome

ORPHA:529965Malformation syndromeAutosomal dominantInfancy

Ассоциированные гены (1)

CHD1
chromodomain helicase DNA binding protein 1
Disease-causing germline mutation(s) in
OMIM: 602118

Фенотипы (19)

Очень частый (80–99%)2
HP:0001263Global developmental delay
HP:0001290Generalized hypotonia
Частый (30–79%)10
HP:0000307Pointed chin
HP:0000494Downslanted palpebral fissures
HP:0000574Thick eyebrow
HP:0001249Intellectual disability
HP:0002007Frontal bossing
HP:0007874Almond-shaped palpebral fissure
HP:0010648Dermal translucency
HP:0011098Speech apraxia
HP:0011800Midface retrusion
HP:0012393Allergy
Периодический (5–29%)7
HP:0000256Macrocephaly
HP:0000729Autistic behavior
HP:0000733Abnormal repetitive mannerisms
HP:0001211Abnormal fingertip morphology
HP:0001250Seizure
HP:0002721Immunodeficiency
HP:0008897Postnatal growth retardation

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