HistoryThis section has been translated automatically.
Lelis J, 1992
DefinitionThis section has been translated automatically.
The main symptoms of this rare, not fully delimited syndrome are hypohidrosis, xeroderma, hypotrichosis, dystrophy of the teeth, benign acanthosis nigricans and lingua plicata. Other symptoms may include mental retardation, nail dystrophy, disorders of skin pigmentation (perioral and periorbital hyperpigmentation, vitiligo), and palmoplantar keratoses.
LiteratureThis section has been translated automatically.
- Lelis J (1992) Autosomal recessive ectodermal dysplasia. Cutis 49:435-437.
- Samdani AJ (2004) Ectodermal dysplasia with acanthosis nigricans (Lelis' syndrome). J Coll Physicians Surg Pak 14:626-627.
Recommended articles
Incoming links (1)
Rasopathies (overview);Outgoing links (6)
Acanthosis nigricans benigna; Hypohidrosis; Hypotrichosis; Lingua plicata; Palmoplantar keratoses (overview); Vitiligo (overview);Disclaimer
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