Disease name

Acrodysostosis
 Acrodysostosis

Marker gene

Gene symbol Chromosome location Protein name
DHODH 16q22 Dihydroorotate dehydrogenase, mitochondrial

Prevalence

미상

Inheritance

상염색체 우성

Age of onset

신생아기, 영아기

ICD 10 code

Q75.4, Q87.0

MIM number

101800

Synonym

Acrodysplasia
Arkless-Graham syndrome
Maroteaux-Malamut syndrome

Summary

Acrodysostosis is an extremely rare disorder characterized by abnormally short and malformed bones of the hands and feet (peripheral dysostosis), nasal hypoplasia and mental retardation. Other findings include progressive growth delays, short stature, unusual head and characteristic facies. Occasionally, abnormal interpedicular spinal spaces, increased mandibular angle and hearing loss have been observed. Widespread epiphyseal stippling and the metacarpophalangeal pattern profile could be useful as diagnostic tools. The aetiology and the prevalence are unknown. Many reported cases are sporadic; some are familial and are transmitted in an autosomal dominant manner. Prenatal diagnosis relies on high-resolution real-time ultrasonography. There is no treatment or specific preventive measures. Consultation with an orthopedist and podiatrist, as well as learning support should be offered.