Literature DB >> 29044700

Epidermal nevus syndromes: New insights into whorls and swirls.

Sarah Asch1, Jeffrey L Sugarman2,3.   

Abstract

Knowledge of the molecular underpinnings of many epidermal nevi and epidermal nevus syndrome has expanded rapidly in recent years. In this review and update on epidermal nevus syndrome, we will cover recent genetic discoveries involving epidermal nevi, including nevus sebaceus, keratinocytic epidermal nevus, nevus comedonicus, congenital hemidysplasia with ichthyosiform nevus and limb defects syndrome, phakomatosis pigmentokeratotica, Becker's nevus, porokeratotic adnexal ostial nevus, inflammatory linear verrucous epidermal nevi, and cutaneous-skeletal hypophosphatemia syndrome. We will discuss how newly defined mutations relate to the biology reflected in the cutaneous patterns seen in these mosaic disorders and how new molecular data has informed our understanding of these diseases and shaped management decisions.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  Becker's nevus; congenital hemidysplasia with ichthyosiform nevus and limb defects syndrome; cutaneous-skeletal hypophosphatemia syndrome; epidermal nevus; inflammatory linear verrucous epidermal nevus; nevus comedonicus; nevus sebaceous; phakomatosis pigmentokeratotica; porokeratotic adnexal ostial nevus

Mesh:

Year:  2017        PMID: 29044700     DOI: 10.1111/pde.13273

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  4 in total

Review 1.  [Syndroms associated with benign skin tumors].

Authors:  George-Sorin Tiplica; Klaus Fritz; Alexandra Irina Butacu; Loredana Ungureanu; Carmen Maria Sălăvăstru
Journal:  Hautarzt       Date:  2022-01-25       Impact factor: 0.751

Review 2.  [Benign skin neoplasms in children].

Authors:  Carmen Maria Salavastru; Alexandra-Irina Butacu; Klaus Fritz; Seher Eren; George-Sorin Tiplica
Journal:  Hautarzt       Date:  2022-01-14       Impact factor: 0.751

Review 3.  DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.

Authors:  Luis F de Castro; Diana Ovejero; Alison M Boyce
Journal:  Eur J Endocrinol       Date:  2020-05       Impact factor: 6.664

4.  Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies.

Authors:  Aude Beyens; Laure Dequeker; Hilde Brems; Sandra Janssens; Hannes Syryn; Anne D'Hooghe; Pascale De Paepe; Lieve Vanwalleghem; Annelies Stockman; Elena Vankwikelberge; Sofie De Schepper; Marleen Goeteyn; Patricia Delbeke; Bert Callewaert
Journal:  Int J Mol Sci       Date:  2022-04-06       Impact factor: 5.923

  4 in total

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