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Growth delay due to insulin-like growth factor I resistance

ORPHA:73273DiseaseAutosomal dominant, Autosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

IGF1R
insulin like growth factor 1 receptor
Disease-causing germline mutation(s) in
OMIM: 147370

Фенотипы (16)

Очень частый (80–99%)4
HP:0001510Growth delay
HP:0001511Intrauterine growth retardation
HP:0002750Delayed skeletal maturation
HP:0004322Short stature
Частый (30–79%)12
HP:0000232Everted lower lip vermilion
HP:0000233Thin vermilion border
HP:0000252Microcephaly
HP:0000319Smooth philtrum
HP:0000431Wide nasal bridge
HP:0000455Broad nasal tip
HP:0000767Pectus excavatum
HP:0001249Intellectual disability
HP:0001270Motor delay
HP:0004279Short palm
HP:0006610Wide intermamillary distance
HP:0030084Clinodactyly

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