Microcephalic osteodysplastic primordial dwarfism type II

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Name:
Microcephalic osteodysplastic primordial dwarfism type II
Description:
A rare bone disease and a form of microcephalic primordial dwarfism characterized by severe pre- and postnatal growth retardation, with marked microcephaly in proportion to body size, skeletal dysplasia, abnormal dentition, insulin resistance, and increased risk for cerebrovascular disease.
ORPHAcode:
2637
Synonyms:
MOPD type II
Majewski osteodysplastic primordial dwarfism type II
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14