Literature DB >> 1918493

How many epidermal nevus syndromes exist? A clinicogenetic classification.

R Happle1.   

Abstract

The term epidermal nevus syndrome is not suitable to describe an entity because there are different birth defects associated with epidermal nevi. A new classification is proposed to distinguish three well-defined syndromes, each recognizable by a different type of nevus. The sebaceous nevus syndrome and the Proteus syndrome are most likely due to autosomal lethal mutations and therefore always occur sporadically, whereas the CHILD syndrome can be transmitted from a mother to her daughter as an X-linked dominant, male-lethal trait. Moreover, the nevus comedonicus syndrome can be regarded as an entity closely related to this group of disorders. It may represent another autosomal lethal mutation that survives by mosaicism. In addition, several less well-defined phenotypes associated with epidermal nevi are reviewed. Some of them are regarded as entities in limbo.

Entities:  

Mesh:

Year:  1991        PMID: 1918493     DOI: 10.1016/0190-9622(91)70238-w

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  6 in total

Review 1.  A genomic view of mosaicism and human disease.

Authors:  Leslie G Biesecker; Nancy B Spinner
Journal:  Nat Rev Genet       Date:  2013-05       Impact factor: 53.242

2.  Angora hair nevus. A further case of an unusual epidermal nevus representing a hallmark of angora hair nevus syndrome.

Authors:  María Del Carmen Boente; Raúl Asial; Norma Beatriz Primc; Rudolf Happle
Journal:  J Dermatol Case Rep       Date:  2013-06-30

3.  Oral HRAS Mutation in Orofacial Nevus Sebaceous Syndrome (Schimmelpenning-Feuerstein-Mims-Syndrome): A Case Report With a Literature Survey.

Authors:  Reinhard E Friedrich; Martin Gosau; Andreas M Luebke; Christian Hagel; Felix K Kohlrusch; Michael Hahn; Simon VON Kroge; Jan Hahn; Ilse Wieland; Martin Zenker
Journal:  In Vivo       Date:  2022 Jan-Feb       Impact factor: 2.155

Review 4.  Ophthalmologic abnormalities in encephalocraniocutaneous lipomatosis.

Authors:  M J MacLaren; I Kluijt; F D Koole
Journal:  Doc Ophthalmol       Date:  1995       Impact factor: 2.379

5.  Hemimegalencephaly with Facial Congenital Infiltrating Lipomatosis in a Child.

Authors:  Adrián Santana-Ramirez; Felipe Farias-Serratos; José Sanchez-Corona; Gema Castañeda-Cisneros; Nadia M Farias-Serratos
Journal:  Iran J Public Health       Date:  2014-12       Impact factor: 1.429

6.  Side differences in the degree of mosaicism of the buccal mucosa in Turner syndrome.

Authors:  Sofia Thunström; Kerstin Landin-Wilhelmsen; Inger Bryman; Charles Hanson
Journal:  Mol Genet Genomic Med       Date:  2019-08-29       Impact factor: 2.183

  6 in total

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