Artículos de revistas
Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome)
Registro en:
American Journal Of Medical Genetics. Wiley-liss, v. 113, n. 4, n. 381, n. 384, 2002.
0148-7299
WOS:000179501400012
10.1002/ajmg.10787
Autor
Steiner, CE
Cintra, ML
Marques-de-Faria, AP
Institución
Resumen
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. 113 4 381 384