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Xq25 microduplication syndrome

ORPHA:521258Malformation syndromeChildhood, Infancy

Ассоциированные гены (1)

STAG2
STAG2 cohesin complex component
Role in the phenotype of
OMIM: 300826

Фенотипы (20)

Частый (30–79%)19
HP:0000272Malar flattening
HP:0000286Epicanthus
HP:0000297Facial hypotonia
HP:0000303Mandibular prognathia
HP:0000729Autistic behavior
HP:0000739Anxiety
HP:0000752Hyperactivity
HP:0001250Seizure
HP:0001263Global developmental delay
HP:0001290Generalized hypotonia
HP:0001321Cerebellar hypoplasia
HP:0002079Hypoplasia of the corpus callosum
HP:0002342Intellectual disability, moderate
HP:0002360Sleep abnormality
HP:0002553Highly arched eyebrow
HP:0008050Abnormality of the palpebral fissures
HP:0009088Speech articulation difficulties
HP:0012471Thick vermilion border
HP:0045075Sparse eyebrow
Периодический (5–29%)1
HP:0004322Short stature

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