Epidermal nevus syndrome: Difference between revisions

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Line 1: {{Infobox medical condition (new) '''Epidermal nevus syndrome''' (also known as "Feuerstein and Mims syndrome," and "Solomon's syndrome"<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0071380760.</ref>{{rp\|775}}) was first described in 1968, and consists of extensive epidermal nevi with abnormalities of the CNS, skeleton, skin, cardiovascular system, gentiourinary system, and eyes.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0721629210.</ref>{{rp\|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<ref name="Happel">Happle, R. "Epidermal nevus syndrome." ''Semin Dermatol''. 1995;14:111.</ref>:▼ \| name = Epidermal nevus syndrome \| synonyms = Solomon's syndrome, Feuerstein and Mims syndrome \| image = Epidermal nevus.jpg \| alt = \| caption = Epidermal nevus in lower eyelid margin \| pronounce = \| field = \| symptoms = \| complications = \| onset = \| duration = \| types = \| causes = \| risks = \| diagnosis = \| differential = \| prevention = \| treatment = \| medication = \| prognosis = \| frequency = \| deaths = }} ▲'''Epidermal nevus syndrome''', (also known as "'''Feuerstein and Mims syndrome''',<ref name="Fitz2" ~~and~~/><ref name="Andrews" /> and '''Solomon's syndrome"'''<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. {{ISBN ~~0071380760~~\|0-07-138076-0}}.</ref>{{rp\|775}})<ref name="Bolognia">{{cite book \|author=Rapini, Ronald P. \|author2=Bolognia, Jean L. \|author3=Jorizzo, Joseph L. \|title=Dermatology: 2-Volume Set \|publisher=Mosby \|location=St. Louis \|year=2007 \|isbn=978-1-4160-2999-1 }}</ref> 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]], ~~gentiourinary~~[[genitourinary system,]] and eyes.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. {{ISBN ~~0721629210~~\|0-7216-2921-0}}.</ref>{{rp\|634}} However, since the syndrome's first description, a broader concept for the "epidermal nevus<!--Q4454468-->" syndrome has been proposed, with at least six types being described:<ref name="Fitz2" />{{rp\|776}}<ref name="Happel">Happle, R. "Epidermal nevus syndrome." ''Semin Dermatol''. 1995;14:111.</ref>: :* [[Schimmelpenning syndrome]] :* [[Nevus comedonicus syndrome]] Line 8 ⟶ 32: ==See also== * [[Epidermis (skin)\|Epidermis]] * [[~~Skin~~List ~~lesion~~of cutaneous conditions]] ==References== {{reflist}} == External links == ~~{{Dermatology-stub}}~~ {{Medical resources [[Category:Epidermal nevi, neoplasms, cysts]]▼ \| ICD10 = Q85.8 \| ICD9 = <!--{{ICD9\|xxx}}--> \| ICDO = \| OMIM = \| DiseasesDB = \| MedlinePlus = \| eMedicineSubj = \| eMedicineTopic = \| MeSH = C536114 \| GeneReviewsNBK = \| GeneReviewsName = \| Orphanet = 35125 }} {{Skin tumors, epidermis}} ▲[[Category:Epidermal nevi, neoplasms, and cysts]] [[Category:Rare syndromes]] {{Epidermal-growth-stub}}