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Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome

ORPHA:71267Malformation syndromeAutosomal recessiveInfancy, Neonatal

Фенотипы (11)

Очень частый (80–99%)11
HP:0000322Short philtrum
HP:0000407Sensorineural hearing impairment
HP:0000426Prominent nasal bridge
HP:0000684Delayed eruption of teeth
HP:0000703Dentinogenesis imperfecta
HP:0000926Platyspondyly
HP:0000939Osteoporosis
HP:0001256Intellectual disability, mild
HP:0001999Abnormal facial shape
HP:0004322Short stature
HP:0010579Cone-shaped epiphysis

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