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Unilateral segmentally arranged basaloid follicular hamartomas with osteoma cutis and hypodontia: a case of Happle–Tinschert syndrome
Author(s) -
Lo C.S.,
Wu Y.F.,
Hsiao Y.W.,
Chung W.H.,
Yang C.H.
Publication year - 2013
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/ced.12161
Subject(s) - medicine , dermatology , hypodontia , dentistry
Summary Happle–Tinschert syndrome ( HTS ) is a rare syndrome characterized by segmentally arranged basaloid follicular hamartomas ( BFH ) associated with ipsilateral osseous, dental and cerebral abnormalities. Happle and Tinschert first reported this disorder in 2008, and three cases with similar presentations have since been reported. We report another case, that of a 40‐year‐old man, presenting with the characteristic clinical features of HTS .