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Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Malformation syndromeInfancy, Neonatal

Фенотипы (17)

Очень частый (80–99%)9
HP:0000268Dolichocephaly
HP:0000486Strabismus
HP:0000768Pectus carinatum
HP:0001166Arachnodactyly
HP:0001249Intellectual disability
HP:0001252Hypotonia
HP:0002650Scoliosis
HP:0002808Kyphosis
HP:0006703Aplasia/Hypoplasia of the lungs
Частый (30–79%)8
HP:0000035Abnormal testis morphology
HP:0000047Hypospadias
HP:0000164Abnormality of the dentition
HP:0001387Joint stiffness
HP:0001608Abnormality of the voice
HP:0002205Recurrent respiratory infections
HP:0002750Delayed skeletal maturation
HP:0007598Bilateral single transverse palmar creases

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