Absence de dermatoglyphes et grains de milium congénitaux : un nouveau cas de syndrome de Basan
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference8 articles.
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2. Ectodermal dysplasia. Missing papillary pattern, nail disorders and furrows on 4 fingers;Basan;Arch Klin Exp Dermatol,1965
3. Congenital absence of dermatoglyphs;Limova;J Am Acad Dermatol,1993
4. Absence of dermal ridge patterns: genetic heterogeneity;Reed;Am J Med Genet,1983
5. Kindred showing congenital absence of the dermal ridges (fingerprints) and associated anomalies;Baird;J Pediatr,1964
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1. Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family;JID Innovations;2021-09
2. Importancia de las lesiones cutáneas benignas transitorias en el recién nacido y su diagnóstico diferencial;Piel;2021-08
3. Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphia;American Journal of Medical Genetics Part A;2018-10-05
4. Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome;European Journal of Human Genetics;2016-03-02
5. Analysis of two candidate genes for Basan syndrome;American Journal of Medical Genetics Part A;2014-03-24
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