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Generalized lentiginosis

From Wikipedia, the free encyclopedia
Generalized lentiginosis
Other namesFamilial multiple lentigines syndrome without systemic involvement[1]
Generalized lentiginosis is inherited in an autosomal dominant manner
SpecialtyDermatology Edit this on Wikidata

Generalized lentiginosis is a cutaneous condition that will occasionally present without other associated abnormalities.[2]: 686  It may be caused by carney complex, Noonan syndrome with multiple lentigines or Peutz–Jeghers syndrome.

See also

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References

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  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Familial generalized lentiginosis". www.orpha.net. Retrieved 20 April 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
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