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]
| Epidermal nevus syndrome | |
|---|---|
| Other names | Solomon's syndrome |
 | |
| Epidermal nevus in lower eyelid margin | |
| Specialty | Dermatology, medical genetics  |
See also edit
References edit
- ^ a b c Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ^ a b James, 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.