Rhizomelic syndrome, Urbach type

Orpha code: 3098OMIM code: 268250

Definition

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
Classification

Malformation syndrome

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

No additional description.

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