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Microcephaly-cardiomyopathy syndrome

ORPHA:2515Malformation syndromeAutosomal recessiveInfancy, Neonatal

Фенотипы (15)

Очень частый (80–99%)4
HP:0000252Microcephaly
HP:0001249Intellectual disability
HP:0001644Dilated cardiomyopathy
HP:0100543Cognitive impairment
Частый (30–79%)4
HP:0000356Abnormality of the outer ear
HP:0001852Sandal gap
HP:0004209Clinodactyly of the 5th finger
HP:0004322Short stature
Периодический (5–29%)7
HP:0000340Sloping forehead
HP:0001250Seizure
HP:0001511Intrauterine growth retardation
HP:0001629Ventricular septal defect
HP:0002119Ventriculomegaly
HP:0002705High, narrow palate
HP:0007703Abnormality of retinal pigmentation

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