Dyggve-Melchior-Clausen Syndrome: A rare genetic bone growth disorder characterized by short stature and other skeletal deformities. More detailed information about the symptoms, causes, and treatments of Dyggve-Melchior-Clausen Syndrome is available below.
See full list of 42 symptoms of Dyggve-Melchior-Clausen Syndrome
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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 Dyggve-Melchior-Clausen Syndrome as a "rare disease".
Source - Orphanet
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