Achondroplasia is the most common cause of disproportionate short stature, caused by mutations in the FGFR3 gene that impair the normal conversion of cartilage into bone at the growth plates of the long bones. It results in short arms and legs relative to the trunk, a large head with a prominent forehead, and normal intelligence and lifespan for most affected individuals. Roughly eighty percent of cases arise from a new mutation in a child of average-height parents rather than being inherited, and the name comes from Greek roots meaning "without cartilage formation," reflecting the condition's effect on bone growth.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) Sources
1. Wikidata: Achondroplasia
WikidataWikidata P279 (body-system: skeletal)Quote, Wikidata P279 (body-system: skeletal)
Subclass of: osteochondrodysplasia
View the Source 2. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVIIQuote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
View the Source 3. Wikipedia: Non-communicable disease
WikipediaInherited/genetic diseases sectionQuote, Inherited/genetic diseases section
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
View the Source 4. Wikipedia: Achondroplasia
Wikipedia- Achondroplasia is a genetic disorder whose primary feature is dwarfism.
Lead section, transmission-route statement
Achondroplasia is a genetic disorder whose primary feature is dwarfism.
View the Source Reader Challenges (0)
No disputes yet. Spotted an error or a better source? Open the first one.
Sign in to dispute this or suggest a correction.