Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome

Orpha code: 313846OMIM code: 614564

Definicja

Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome is a rare, inherited cancer-predisposing syndrome characterized by an early development of cutaneous telangiectasia, mild dental and nail anomalies, patchy alopecia over the affected skin areas and increased lifetime risk for oropharyngeal cancer. Other types of cancer have also been reported.

Disease data
Klasyfikacja

Disease

Kod ORPHA
313846
Kod OMIM
614564
Kod ICD10
-
Kod ICD11
-

No additional description.

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