Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disease · Growth hormone insensitivity syndrome
Growth delay due to insulin-like growth factor I resistance
Growth delay due to IGF-I resistance is characterized by variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Addition features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum).
This condition has no sub-types.