Ectodermal Dysplasia With Acanthosis Nigricans (lelis Syndrome).

dc.creatorSteiner, Carlos Eduardo
dc.creatorCintra, Maria Letícia
dc.creatorMarques-de-Faria, Antonia Paula
dc.date2002-Dec
dc.date2015-11-27T12:49:24Z
dc.date2015-11-27T12:49:24Z
dc.date.accessioned2018-03-29T00:56:44Z
dc.date.available2018-03-29T00:56:44Z
dc.identifierAmerican Journal Of Medical Genetics. v. 113, n. 4, p. 381-4, 2002-Dec.
dc.identifier0148-7299
dc.identifier10.1002/ajmg.b.10787
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/12457412
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/195205
dc.identifier12457412
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1295438
dc.descriptionA 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.
dc.description113
dc.description381-4
dc.languageeng
dc.relationAmerican Journal Of Medical Genetics
dc.relationAm. J. Med. Genet.
dc.rightsfechado
dc.rightsCopyright 2002 Wiley-Liss, Inc.
dc.sourcePubMed
dc.subjectAbnormalities, Multiple
dc.subjectAcanthosis Nigricans
dc.subjectAdult
dc.subjectDiagnosis, Differential
dc.subjectEctodermal Dysplasia
dc.subjectHumans
dc.subjectIntellectual Disability
dc.subjectKeratoderma, Palmoplantar
dc.subjectMale
dc.subjectSyndrome
dc.titleEctodermal Dysplasia With Acanthosis Nigricans (lelis Syndrome).
dc.typeArtículos de revistas


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