Literature DB >> 30871534

Genotype-phenotype correlations in FSHD.

Nikolay Zernov1, Mikhail Skoblov2,3.   

Abstract

BACKGROUND: Facial-scapular-humeral myodystrophy Landouzy-Dejerine (FSHD) is an autosomal dominant disease, the basis of its pathogenesis is ectopic expression of the transcription factor DUX4 in skeletal muscle. There are two types of the disease: FSHD1 (MIM:158900) and FSHD2 (MIM: 158901), which have different genetic causes but are phenotypically indistinguishable. In FSHD1, partial deletion of the D4Z4 repeats on the 4th chromosome affects the expression of DUX4, whereas FSHD2 is caused by the mutations in the protein regulating the methylation status of chromatin - SMCHD1. High variability of clinical picture, both intra - and inter-family indicates a large number of factors influencing clinical picture. There are key genetic, epigenetic and gender factors that influence the expressivity and penetrance of the disease. Using only one of these factors allows just a rough prediction of the course of the disease, which indicates the combined effect of all of the factors on the DUX4 expression and on the clinical picture.
RESULTS: In this paper, we analyzed the impact of genetic, epigenetic and gender differences on phenotype and the possibility of using them for disease prognosis and family counselling.
CONCLUSIONS: Key pathogenesis factors have been identified for FSHD. However, the pronounced intra - and inter-family polymorphism of manifestations indicates a large number of modifiers of the pathological process, many of which remain unknown.

Entities:  

Keywords:  Anticipation; D4Z4; FSHD; Genotype-phenotype correlation; Inherited disease; Methylation

Year:  2019        PMID: 30871534      PMCID: PMC6416831          DOI: 10.1186/s12920-019-0488-5

Source DB:  PubMed          Journal:  BMC Med Genomics        ISSN: 1755-8794            Impact factor:   3.063


  53 in total

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5.  A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.

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7.  Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element.

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Journal:  Am J Hum Genet       Date:  2012-04-06       Impact factor: 11.025

9.  Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample.

Authors:  M L Mostacciuolo; E Pastorello; G Vazza; M Miorin; C Angelini; G Tomelleri; G Galluzzi; C P Trevisan
Journal:  Clin Genet       Date:  2009-03-23       Impact factor: 4.438

10.  SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation.

Authors:  Marnie E Blewitt; Anne-Valerie Gendrel; Zhenyi Pang; Duncan B Sparrow; Nadia Whitelaw; Jeffrey M Craig; Anwyn Apedaile; Douglas J Hilton; Sally L Dunwoodie; Neil Brockdorff; Graham F Kay; Emma Whitelaw
Journal:  Nat Genet       Date:  2008-04-20       Impact factor: 38.330

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6.  Muscle Fiber Conduction Velocity Correlates With the Age at Onset in Mild FSHD Cases.

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7.  Orofacial Muscle Weakening in Facioscapulohumeral Muscular Dystrophy (FSHD) Patients.

Authors:  Dimitrios Konstantonis; Kyriaki Kekou; Petros Papaefthymiou; Heleni Vastardis; Nikoleta Konstantoni; Maria Athanasiou; Maria Svingou; Anastasia Margariti; Angeliki Panousopoulou
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