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Tetrasomy 21 syndrome

ORPHA:96055Malformation syndromeAntenatal, Infancy, Neonatal

Фенотипы (17)

Частый (30–79%)11
HP:0000248Brachycephaly
HP:0000252Microcephaly
HP:0000311Round face
HP:0000474Thickened nuchal skin fold
HP:0000582Upslanted palpebral fissure
HP:0000954Single transverse palmar crease
HP:0001156Brachydactyly
HP:0001249Intellectual disability
HP:0001252Hypotonia
HP:0001263Global developmental delay
HP:0010808Protruding tongue
Периодический (5–29%)6
HP:0000158Macroglossia
HP:0000316Hypertelorism
HP:0001674Complete atrioventricular canal defect
HP:0001852Sandal gap
HP:0005280Depressed nasal bridge
HP:0005534Transient myeloproliferative syndrome

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