نتایج جستجو برای: epidermal nevus syndrome

تعداد نتایج: 679851  

Journal: :Indian Journal of Dermatology 2015

Journal: :JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH 2015

Journal: :middle east journal of digestive diseases 0
mohammad javad zahedi sodaif darvish moghadam seyed mahdi seyed mirzaei masood dehghani sara shafiei pour atefe rasti

blue rubber bleb nevus syndrome is a rare disorder that is characterized by multiple recurrent vascular malformations of skin and gastrointestinal tract . the affected patients may present with diverse manifestations including iron deficiency anemia. we report this syndrome in a 22-year-old man that was referred to our hospital for iron deficiency anemia with unknown cause and vascular malforma...

Journal: :Archives of dermatology 2010
Gabriel F Sciallis Andrew P Sciallis

BACKGROUND Becker nevus is a nevoid melanosis, referred to as Becker nevus syndrome when it is associated with other anomalies. Our objectives were to report the occurrence of a Becker nevus with an underlying desmoid soft-tissue tumor; to review Mayo Clinic's experience with Becker nevi, concentrating on Becker nevi associated with bone, vascular, neural, and other soft-tissue abnormalities; t...

2013
Serap Gozel Melahat Donmez Noyan Can Akdur Hulya Yikilkan

Nevus sebaceus of Jadassohn is a congenital cutaneous hamartoma comprised of multiple skin structures. It has the potential to develop into variety of neoplasms of various epidermal adnexal origins. While multiple tumors may occasionally arise, it is unusual for more than four tumors to arise simultaneously within a single sebaceus nevus. Here in, we report a case of a 70-year-old woman with si...

Journal: :Cancer research 2004
Mariateresa Mancuso Simonetta Pazzaglia Mirella Tanori Heidi Hahn Paola Merola Simonetta Rebessi Michael J Atkinson Vincenzo Di Majo Vincenzo Covelli Anna Saran

Loss-of-function mutations in Patched (Ptch1) are implicated in constitutive activation of the Sonic hedgehog pathway in human basal cell carcinomas (BCCs), and inherited Ptch1 mutations underlie basal cell nevus syndrome in which a typical feature is multiple BCC occurring with greater incidence in portals of radiotherapy. Mice in which one copy of Ptch1 is inactivated show increased susceptib...

Journal: :Medical Journal Armed Forces India 2015

Journal: :The Journal of investigative dermatology 2007
Akiko Tsubota Masashi Akiyama Kaori Sakai Maki Goto Yukiko Nomura Satomi Ando Masataka Abe Daisuke Sawamura Hiroshi Shimizu

Since 1994, four cases of epidermal nevus with epidermolytic hyperkeratosis (EH) caused by keratin 10 gene mutations have been reported, although no keratin 1 (K1) gene mutation has yet been reported. We detected a K1 gene (KRT1) mutation in epidermal nevus with EH in a 10-year-old Japanese male. The patient showed well-demarcated verrucous, hyperkeratotic plaques mainly on the trunk, covering ...

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