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Microcephalic osteodysplastic primordial dwarfism type II

Congenital Malformations and Chromosomal Abnormalities

Microcephalic osteodysplastic primordial dwarfism type II, often shortened to MOPD II or MOPDII and also called Majewski osteodysplastic primordial dwarfism type II, is a rare inherited condition marked by very short stature, skeletal differences and an unusually small head. Growth is restricted from before birth, so affected infants are small at delivery and keep growing slowly afterward; adult height is reported as roughly 20 to 40 inches. Skeletal findings include hip dysplasia, thin limb bones, scoliosis and shortened wrist bones, and head growth slows over time although intellectual development is typically normal. Many people also have blood vessel abnormalities such as intracranial aneurysm or Moyamoya disease, which raise the risk of stroke. The cause is mutation in the PCNT gene, which encodes pericentrin, a centrosome protein needed for cell division, and inheritance is autosomal recessive. Prevalence is unknown. This entry records what is described and offers no medical advice.

Facts
Classification
Body System
Skeletal System 1
Body System
Cardiovascular System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. Microcephalic osteodysplastic primordial dwarfism type II (MedlinePlus Genetics)
  • Description
    Other skeletal abnormalities in MOPDII include abnormal development of the hip joints (hip dysplasia)
  • Description [body-system]
    Many individuals with MOPDII have blood vessel abnormalities.
  • Causes
    Mutations in the PCNT gene cause MOPDII.
  • Inheritance
    This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations.
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2. EMBL-EBI Ontology Lookup Service: microcephalic osteodysplastic primordial dwarfism type II (DOID term)
EMBL-EBI Ontology Lookup Servicedatabase_cross_reference of the DOID term microcephalic osteodysplastic primordial dwarfism type II; ICD-10 chapter derived from code Q87.1 (WHO range Q00-Q99)
Quote, database_cross_reference of the DOID term microcephalic osteodysplastic primordial dwarfism type II; ICD-10 chapter derived from code Q87.1 (WHO range Q00-Q99)
ICD10CM:Q87.1
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