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Proximal Xq28 duplication syndrome

ORPHA:1762Malformation syndromeAntenatal, Neonatal

Ассоциированные гены (1)

MECP2
methyl-CpG binding protein 2
Role in the phenotype of
OMIM: 300005

Фенотипы (18)

Очень частый (80–99%)14
HP:0000028Cryptorchidism
HP:0000047Hypospadias
HP:0000508Ptosis
HP:0002167Abnormality of speech or vocalization
HP:0002750Delayed skeletal maturation
HP:0002916Abnormality of chromosome segregation
HP:0004322Short stature
HP:0010864Intellectual disability, severe
HP:0000232Everted lower lip vermilion
HP:0000286Epicanthus
HP:0000581Blepharophimosis
HP:0001263Global developmental delay
HP:0010804Tented upper lip vermilion
HP:0011344Severe global developmental delay
Частый (30–79%)3
HP:0000767Pectus excavatum
HP:0001288Gait disturbance
HP:0004299Hernia of the abdominal wall
Периодический (5–29%)1
HP:0001387Joint stiffness

Эпидемиология (3)

Point prevalence
Unknown
Europe
Prevalence at birth
1-9 / 1 000 000
Australia
Annual incidence
<1 / 1 000 000
Australia

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы