Chondrodysplasia Punctata, Rhizomelic type: A rare genetic disorder characterized by slow growth, mental deficiency, characteristic facial features and skeletal deformities particularly of the limbs, spine and pelvis. More detailed information about the symptoms, causes, and treatments of Chondrodysplasia Punctata, Rhizomelic type is available below.
See full list of 18 symptoms of Chondrodysplasia Punctata, Rhizomelic type
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Chondrodysplasia Punctata, Rhizomelic type as a "rare disease".
Source - Orphanet
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