Literature DB >> 31831114

Café au Lait Macules and Associated Genetic Syndromes.

Sharon Anderson.   

Abstract

Café au lait macules (CALMs) are a common, isolated dermatologic finding in the general population. But when do these irregularly shaped, jagged-edged, flat, hyperpigmented birthmarks suggest something that may warrant referral? Most pediatric providers are familiar with the association of CALMs and neurofibromatosis type 1. There are, however, other genetic conditions associated with these seemingly benign skin spots. This article provides an overview of CALMs, followed by a summary of several conditions associated with CALMs ranging from the most common (neurofibromatosis type 1) to rare, ring chromosome syndromes. It reviews the associated gene(s), pattern of inheritance, incidence, presenting symptoms, diagnosis, and management for these genetic conditions.
Copyright © 2019 National Association of Pediatric Nurse Practitioners. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Café au lait macule; Legius syndrome; McCune-Albright syndrome; Noonan syndrome with multiple lentigines; neurofibromatosis type 1

Mesh:

Year:  2020        PMID: 31831114     DOI: 10.1016/j.pedhc.2019.05.001

Source DB:  PubMed          Journal:  J Pediatr Health Care        ISSN: 0891-5245            Impact factor:   1.812


  5 in total

Review 1.  Physical Examination for Endocrine Diseases: Does It Still Play a Role?

Authors:  Andrea Crafa; Rosita A Condorelli; Rossella Cannarella; Antonio Aversa; Aldo E Calogero; Sandro La Vignera
Journal:  J Clin Med       Date:  2022-05-05       Impact factor: 4.964

2.  Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

Authors:  Valentina Orlandi; Paolo Cavarzere; Laura Palma; Rossella Gaudino; Franco Antoniazzi
Journal:  Ital J Pediatr       Date:  2021-03-04       Impact factor: 2.638

3.  McCune-Albright syndrome - A case report with transmission electron microscopy.

Authors:  Victor Garcia Neto; Hiram Larangeira de Almeida; Claúdia Fernandes Lorea; Valéria Magalhães Jorge; Antônia Larangeira de Almeida
Journal:  An Bras Dermatol       Date:  2021-11-25       Impact factor: 1.896

Review 4.  Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants.

Authors:  Hildegard Kehrer-Sawatzki; David N Cooper
Journal:  Hum Genet       Date:  2021-12-20       Impact factor: 4.132

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

  5 in total

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