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Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome) by Carlos Eduardo Steiner; Maria Letícia Cintra; Antonia Paula Marques‐de‐Faria is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome) about?

## 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.

Who reads Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome)?

Author

Carlos Eduardo Steiner; Maria Letícia Cintra; Antonia Paula Marques‐de‐Faria

Publisher

John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 0148-7299)

Published

2002

Language

EN

Field

Biochemistry, Genetics and Molecular Biology (Life Sciences)