Literature DB >> 22980764

Selective pattern of muscle involvement seen in distal muscular dystrophy associated with anoctamin 5 mutations: a follow-up muscle MRI study.

Ibrahim Mahjneh1, Rumaisa Bashir, Sari Kiuru-Enari, Wim Linssen, Antti Lamminen, Marianne de Visser.   

Abstract

Anoctaminopathy is a new muscular dystrophy caused by mutations in the ANO5 gene. ANO5 mutations cause distal and proximal phenotypes. We report here a follow-up muscle MRI study on five patients affected by distal form of anoctaminopathy. T1 weighted scans showed subsequent involvement of gastrocnemius medialis and soleus, hip adductors, hamstrings, gastrocnemius lateralis and quadriceps muscles, and later on tensor fascia lata, gluteus minimus and biceps brachii muscles, respectively. The STIR weighted images showed in the early stages widely distributed hyperintense signals, myoedema, in the adductors, hamstrings, and quadriceps muscles, which at that time have normal T1 signals. All patients showed asymmetry of muscle involvement both clinically and on muscle imaging. The progression of muscle involvement was relatively slow. We conclude that the pattern of muscle involvement seen in patients with distal myopathy with anoctamin 5 mutations (MMD3) is typical and can thus be useful during the differential diagnosis process allowing for a more targeted molecular approach.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22980764     DOI: 10.1016/j.nmd.2012.02.007

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  8 in total

Review 1.  Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review.

Authors:  Doris G Leung
Journal:  J Neurol       Date:  2016-11-25       Impact factor: 4.849

2.  Muscle MRI in muscular dystrophies.

Authors:  Jordi Díaz-Manera; Jaume Llauger; Eduard Gallardo; Isabel Illa
Journal:  Acta Myol       Date:  2015-12

Review 3.  Modulating Ca²⁺ signals: a common theme for TMEM16, Ist2, and TMC.

Authors:  Karl Kunzelmann; Ines Cabrita; Podchanart Wanitchakool; Jiraporn Ousingsawat; Lalida Sirianant; Roberta Benedetto; Rainer Schreiber
Journal:  Pflugers Arch       Date:  2015-12-23       Impact factor: 3.657

4.  Clinical and genetic features of anoctaminopathy in Saudi Arabia.

Authors:  Saeed Bohlega; Dorothy M Monies; Ahmad A Abulaban; Hatem N Murad; Hindi N Alhindi; Brian F Meyer
Journal:  Neurosciences (Riyadh)       Date:  2015-04       Impact factor: 0.906

5.  Whole-body muscle MRI of patients with MATR3-associated distal myopathy reveals a distinct pattern of muscular involvement and highlights the value of whole-body examination.

Authors:  Alexander Mensch; Torsten Kraya; Felicitas Koester; Tobias Müller; Dietrich Stoevesandt; Stephan Zierz
Journal:  J Neurol       Date:  2020-05-02       Impact factor: 4.849

Review 6.  ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies.

Authors:  Jon Christiansen; Anne-Katrin Güttsches; Ulrike Schara-Schmidt; Matthias Vorgerd; Christoph Heute; Corinna Preusse; Werner Stenzel; Andreas Roos
Journal:  Genes Dis       Date:  2022-02-14

7.  The Diagnostic Value of MRI Pattern Recognition in Distal Myopathies.

Authors:  Enrico Bugiardini; Jasper M Morrow; Sachit Shah; Claire L Wood; David S Lynch; Alan M Pitmann; Mary M Reilly; Henry Houlden; Emma Matthews; Matt Parton; Michael G Hanna; Volker Straub; Tarek A Yousry
Journal:  Front Neurol       Date:  2018-06-26       Impact factor: 4.003

8.  Multi-slice MRI reveals heterogeneity in disease distribution along the length of muscle in Duchenne muscular dystrophy.

Authors:  Stephen M Chrzanowski; Celine Baligand; Rebecca J Willcocks; Jasjit Deol; Ilona Schmalfuss; Donovan J Lott; Michael J Daniels; Claudia Senesac; Glenn A Walter; Krista Vandenborne
Journal:  Acta Myol       Date:  2017-09-01
  8 in total

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