Rhizomelic syndrome, Urbach type

Orpha code: 3098OMIM code: 268250

Definicja

Rhizomelic syndrome, Urbach type is a rare primary bone dysplasia characterized by upper limbs rhizomelia and other skeletal anomalies (e.g. short stature, dislocated hips, digitalization of the thumb with bifid distal phalanx), craniofacial features (e.g. microcephaly, large anterior fontanelle, fine and sparse scalp hair, depressed nasal bridge, high arched palate, micrognathia, short neck), congenital heart defects (e.g. pulmonary stenosis), delayed psychomotor development and mild flexion contractures of elbows. Radiologic evaluation may reveal flared epiphyses, platyspondyly and/or digital anomalies.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
3098
Kod OMIM
268250
Kod ICD10
Q87.1
Kod ICD11
-

No additional description.

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