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Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome)

✍ Scribed by Steiner, Carlos Eduardo ;Cintra, Maria Let�cia ;Marques-de-Faria, Antonia Paula

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
180 KB
Volume
113
Category
Article
ISSN
0148-7299

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✦ Synopsis

Abstract

A 31‐year‐old male patient with ectodermal dysplasia and acanthosis nigricans is described. Clinical findings included hypotrichosis, hypohidrosis, palmoplantar hyperkeratosis, nail dystrophy, early onset loss of permanent dentition, mental retardation, and acanthosis nigricans. The findings suggest the diagnosis of Lelis syndrome, as described on the basis of seven unrelated cases. A review concerning this condition is also presented. © 2002 Wiley‐Liss, Inc.

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