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Condition

Acrodysostosis

Congenital Malformations and Chromosomal Abnormalities

Acrodysostosis is a rare congenital malformation syndrome. It involves shortening of the interphalangeal joints of the hands and feet, intellectual disability in approximately 90 percent of affected children, and peculiar facial features. Other common abnormalities include a short head as measured front to back, a small broad upturned nose with a flat nasal bridge, a protruding jaw, increased bone age, intrauterine growth retardation, juvenile arthritis and short stature. Further abnormalities of the skin, genitals, teeth and skeleton may also occur, so the condition affects several body systems at once and is recognised by this combined pattern rather than by any single finding.

Facts
Classification
Body System
Skeletal System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 3
Sources
1. Acrodysostosis (Wikipedia)
Lead paragraph
Quote, Lead paragraph
shortening of the interphalangeal joints of the hands and feet
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2. World Health Organization: ICD-10 Version:2019 - Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
World Health OrganizationCategory Q75.4
Quote, Category Q75.4
Q75.4 Mandibulofacial dysostosis
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3. Orphanet (INSERM): Orphanet: Acrodysostosis (ORPHA:950)
Orphanet (INSERM)DisorderGeneAssociation
Quote, DisorderGeneAssociation
"DisorderGeneAssociationType": "Disease-causing germline mutation(s) in"
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