Literature DB >> 29432239

Neurocutaneous Disorders.

Tena Rosser.   

Abstract

PURPOSE OF REVIEW: This article presents an up-to-date summary of the genetic etiology, diagnostic criteria, clinical features, and current management recommendations for the most common neurocutaneous disorders encountered in clinical adult and pediatric neurology practices. RECENT
FINDINGS: The phakomatoses are a phenotypically and genetically diverse group of multisystem disorders that primarily affect the skin and central nervous system. A greater understanding of the genetic and biological underpinnings of numerous neurocutaneous disorders has led to better clinical characterization, more refined diagnostic criteria, and improved treatments in neurofibromatosis type 1, Legius syndrome, neurofibromatosis type 2, Noonan syndrome with multiple lentigines, tuberous sclerosis complex, Sturge-Weber syndrome, and incontinentia pigmenti.
SUMMARY: Neurologists require a basic knowledge of and familiarity with a wide variety of neurocutaneous disorders because of the frequent involvement of the central and peripheral nervous systems. A simple routine skin examination can often open a broad differential diagnosis and lead to improved patient care.

Entities:  

Mesh:

Year:  2018        PMID: 29432239     DOI: 10.1212/CON.0000000000000562

Source DB:  PubMed          Journal:  Continuum (Minneap Minn)        ISSN: 1080-2371


  6 in total

Review 1.  Dermatologic Symptoms and Syndromes Associated with Headache.

Authors:  Arathi Nandyala; Carrie Dougherty
Journal:  Curr Pain Headache Rep       Date:  2022-09-06

2.  Maternal smoking during pregnancy and risk of phacomatoses: results from a Swedish register-based study.

Authors:  Giorgio Tettamanti; Hanna Mogensen; Ann Nordgren; Maria Feychting
Journal:  Clin Epidemiol       Date:  2019-09-03       Impact factor: 4.790

3.  Blue Rubber Bleb Nevus Syndrome With Multiple Cavernoma-Like Lesions on MRI: A Familial Case Report and Literature Review.

Authors:  García Anwár; Paredes-Aragón Elma; Jorge-de Saráchaga Adib; Meyer-Nava Ilse; Gutiérrez-Romero Alonso; Salinas Lara Ciltlaltepelt; Novelo Soto Alma; Vega Memije Maria Elisa; Arauz Antonio
Journal:  Front Neurol       Date:  2020-04-07       Impact factor: 4.003

4.  Consensus Statement for the Management and Treatment of Sturge-Weber Syndrome: Neurology, Neuroimaging, and Ophthalmology Recommendations.

Authors:  Sara Sabeti; Karen L Ball; Sanjoy K Bhattacharya; Elena Bitrian; Lauren S Blieden; James D Brandt; Craig Burkhart; Harry T Chugani; Stephen J Falchek; Badal G Jain; Csaba Juhasz; Jeffrey A Loeb; Aimee Luat; Anna Pinto; Eric Segal; Jonathan Salvin; Kristen M Kelly
Journal:  Pediatr Neurol       Date:  2021-05-06       Impact factor: 4.210

5.  Diagnostic difficulties and possibilities of NF1-like syndromes in childhood.

Authors:  Eva Pinti; Krisztina Nemeth; Krisztina Staub; Anna Lengyel; Gyorgy Fekete; Iren Haltrich
Journal:  BMC Pediatr       Date:  2021-07-29       Impact factor: 2.125

Review 6.  Consensus Statement for the Management and Treatment of Port-Wine Birthmarks in Sturge-Weber Syndrome.

Authors:  Sara Sabeti; Karen L Ball; Craig Burkhart; Lawrence Eichenfield; Esteban Fernandez Faith; Ilona J Frieden; Roy Geronemus; Deepti Gupta; Andrew C Krakowski; Moise L Levy; Denise Metry; J Stuart Nelson; Megha M Tollefson; Kristen M Kelly
Journal:  JAMA Dermatol       Date:  2021-01-01       Impact factor: 10.282

  6 in total

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