Dermatoosteolysis, Kirghizian type: A rare condition characterized by a variety of abnormalities including missing teeth, recurring skin ulceration, eye problems and nail symptoms. More detailed information about the symptoms, causes, and treatments of Dermatoosteolysis, Kirghizian type is available below.
See full list of 12 symptoms of Dermatoosteolysis, Kirghizian type
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Dermatoosteolysis, Kirghizian type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Dermatoosteolysis, Kirghizian type, or a subtype of Dermatoosteolysis, Kirghizian type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Dermatoosteolysis, Kirghizian type as a "rare disease".
Source - Orphanet
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