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Pentasomy X syndrome

ORPHA:11Malformation syndromeNeonatal

Фенотипы (22)

Очень частый (80–99%)2
HP:0001252Hypotonia
HP:0000358Posteriorly rotated ears
Частый (30–79%)15
HP:0000252Microcephaly
HP:0000316Hypertelorism
HP:0000347Micrognathia
HP:0000431Wide nasal bridge
HP:0000486Strabismus
HP:0000582Upslanted palpebral fissure
HP:0001249Intellectual disability
HP:0001263Global developmental delay
HP:0001357Plagiocephaly
HP:0001773Short foot
HP:0002974Radioulnar synostosis
HP:0004209Clinodactyly of the 5th finger
HP:0004322Short stature
HP:0100490Camptodactyly of finger
HP:0200055Small hand
Периодический (5–29%)5
HP:0000823Delayed puberty
HP:0001385Hip dysplasia
HP:0001643Patent ductus arteriosus
HP:0001671Abnormal cardiac septum morphology
HP:0010978Abnormality of immune system physiology

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы