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17q11.2 microduplication syndrome

ORPHA:139474Malformation syndromeAutosomal dominantInfancy, Neonatal

Ассоциированные гены (1)

NF1
neurofibromin 1
Role in the phenotype of
OMIM: 613113

Фенотипы (16)

Частый (30–79%)6
HP:0000252Microcephaly
HP:0000682Abnormality of dental enamel
HP:0001249Intellectual disability
HP:0001263Global developmental delay
HP:0004322Short stature
HP:0006297Enamel hypoplasia
Периодический (5–29%)10
HP:0000053Macroorchidism
HP:0000233Thin vermilion border
HP:0000272Malar flattening
HP:0000653Sparse eyelashes
HP:0000750Delayed speech and language development
HP:0001250Seizure
HP:0004411Deviated nasal septum
HP:0009928Thick nasal alae
HP:0011803Bifid nose
HP:0045075Sparse eyebrow

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