期刊
CLINICAL CASE REPORTS
卷 10, 期 3, 页码 -出版社
WILEY
DOI: 10.1002/ccr3.5577
关键词
ectodermal dysplasia; hypohidrotic; keratoderma; Rapp-Hodgkin
Rapp-Hodgkin syndrome (RHS) is a rare condition characterized by ectodermal dysplasia and palatal abnormalities. This case report describes a 15-year-old boy with RHS associated with palmoplantar keratoderma (PPK).
Rapp-Hodgkin syndrome (RHS) is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. Palmoplantar keratoderma (PPK) is an unusual manifestation of hidrotic ED. Ulcerations on the palms are also not common in RHS. We describe a 15-year-old boy who has RHS associated with PPK.
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