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]
Schimmelpenning syndrome
Nevus comedonicus syndrome
Pigmented hairy epidermal nevus syndrome
Proteus syndrome
CHILD syndrome
Phakomatosis pigmentokeratotica
^ abcFreedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
^ abJames, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
^Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
^Happle, R. "Epidermal nevus syndrome." Semin Dermatol. 1995;14:111.
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"Solomon syndrome", and "Jadassohn's nevus phakomatosis". "Nevus" is sometimes spelled "naevus" and "sebaceous" may also be spelled "sebaceus". "Epidermal nevus...
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Sebaceous nevussyndrome is a cutaneous condition and may resemble CHILD syndrome. Sebaceous hyperplasia List of cutaneous conditions Rapini, Ronald P...
1980). "Leukoedema of the oral mucosa. Possibly an acquired white sponge nevus". Archives of Dermatology. 116 (8): 906–8. doi:10.1001/archderm.1980.01640320056014...
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