Lelis syndrome Q82.4

Last updated on: 22.07.2021

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History
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Lelis J, 1992

Definition
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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.

Literature
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  1. Lelis J (1992) Autosomal recessive ectodermal dysplasia. Cutis 49:435-437.
  2. Samdani AJ (2004) Ectodermal dysplasia with acanthosis nigricans (Lelis' syndrome). J Coll Physicians Surg Pak 14:626-627.

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Disclaimer

Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

Last updated on: 22.07.2021