Dyskeratosis congenita: Difference between revisions

Revision as of 15:45, 24 July 2012

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

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-{{CMG}}
+{{Infobox Disease
+| Name = Dyskeratosis congenita
-{{EH}}
+| Image =
+| Caption =
-'''Dyskeratosis congenita''' (DKC) is a rare progressive [[bone marrow]] failure syndrome characterized by cutaneous pigmentation, [[dystrophy]] of the [[nail (anatomy)|nail]]s, [[leukoplakia]] of the oral mucosa, continuous lacrimation due to [[atresia]] of the [[lacrimal duct]]s, often [[thrombocytopenia]], anemia and in most cases [[testicular atrophy]]. People afflicted with this are also highly susceptible to developing cancer.
+| DiseasesDB = 30105
-{{WH}}
+| ICD10 = {{ICD10|Q|82|8|q|80}}
-{{WS}}
+| ICD9 = {{ICD9|757.39}}
+| ICDO =
-[[Category:Disease]]
+| OMIM = 305000
+| MedlinePlus =
+| eMedicineSubj = derm
+| eMedicineTopic = 111
+| MeshID = D019871
+}}
+{{CMG}} {{AE}} {{RT}}