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Campomelic dysplasia

Congenital Malformations and Chromosomal Abnormalities

Campomelic dysplasia, abbreviated CMD, is a genetic disorder characterized by bowing of the long bones along with many other skeletal and extraskeletal features. It can be lethal in the newborn period because of respiratory insufficiency, but severity varies and a significant proportion of patients survive into adulthood. The name comes from the Greek roots campo, meaning bent, and melia, meaning limb. Up to two thirds of affected 46,XY genotypic males show disorders of sexual development with ambiguous genitalia, and some develop as phenotypic females. An atypical form without bowed limbs, called acampomelic campomelic dysplasia, occurs in about ten percent of patients, particularly those who survive the newborn period.

Facts
Classification
Body System
Skeletal System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 3
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Prevalence Band
Rare (Under 1 in 2000) 4
Sources
1. Campomelic dysplasia (Wikipedia)
  • Lead, first sentence
    is a genetic disorder characterized by bowing of the long bones
  • Lead, first sentence [body-system]
    bowing of the long bones and many other skeletal and extraskeletal features
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2. National Cancer Institute (NCI Thesaurus): Campomelic dysplasia - NCI Thesaurus concept C84609
National Cancer Institute (NCI Thesaurus)Definition
Quote, Definition
A genetic congenital disorder characterized by bowing and angulation of the long bones.
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3. MedlinePlus Genetics (U.S. National Library of Medicine): Campomelic dysplasia - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and Inheritance
Quote, Description and Inheritance
Campomelic dysplasia is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
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4. Orphadata (Orphanet): Orphadata epidemiology, ORPHAcode 140
Orphadata (Orphanet)Orphanet epidemiology, ORPHAcode 140
Quote, Orphanet epidemiology, ORPHAcode 140
"PrevalenceClass": "\u003c1 / 1 000 000", "PrevalenceGeographic": "Worldwide", "PrevalenceQualification": "Value and class", "PrevalenceType": "Point prevalence"
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