Please use this identifier to cite or link to this item:
|Type:||Artigo de periódico|
|Title:||Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome)|
|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. (C) 2002 Wiley-Liss, Inc.|
|Citation:||American Journal Of Medical Genetics. Wiley-liss, v. 113, n. 4, n. 381, n. 384, 2002.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.