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Epidermal nevus syndrome

From Wikipedia, the free encyclopedia

Epidermal nevus syndrome
Other namesSolomon's syndrome
Epidermal nevus in lower eyelid margin
SpecialtyDermatology, medical genetics Edit this on Wikidata

Epidermal nevus syndrome (also known as "Feuerstein and Mims syndrome",[1][2] and "Solomon's syndrome"[1]: 775 [3]) is a rare disease that was first described in 1968 and consists of extensive epidermal nevi with abnormalities of the central nervous system (CNS), skeleton, skin, cardiovascular system, genitourinary system and eyes.[2]: 634  However, since the syndrome's first description, a broader concept for the "epidermal nevus" syndrome has been proposed, with at least six types being described:[1]: 776 [4]

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Transcription

See also

References

  1. ^ a b c Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
  2. ^ a b James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  3. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
  4. ^ Happle, R. "Epidermal nevus syndrome." Semin Dermatol. 1995;14:111.

External links


This page was last edited on 3 April 2024, at 22:05
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