Literature DB >> 17620497

Limb-girdle muscular dystrophy due to emerin gene mutations.

Shigehisa Ura1, Yukiko K Hayashi, Kanako Goto, Mina Nolasco Astejada, Terumi Murakami, Masako Nagato, Shigeru Ohta, Yasuhisa Daimon, Hidehiro Takekawa, Koichi Hirata, Ikuya Nonaka, Satoru Noguchi, Ichizo Nishino.   

Abstract

BACKGROUND: Emery-Dreifuss muscular dystrophy, caused by EMD gene mutations, is characterized by humeroperoneal muscular dystrophy, joint contractures, and conduction defects and is often associated with sudden cardiac death, even without prior cardiac symptoms.
OBJECTIVE: To describe the clinical and molecular features of 2 patients with limb-girdle muscular dystrophy with mutations in EMD.
DESIGN: Case reports.
SETTING: Academic research. PATIENTS: Two male patients manifested proximal dominant muscle involvement, with minimal or no joint and cardiac involvement. MAIN OUTCOME MEASURES: Muscle biopsy and mutation analysis results.
RESULTS: Immunohistochemistry revealed an absence of emerin staining in muscle biopsy specimens. Mutation analysis identified nonsense mutations in EMD.
CONCLUSIONS: Mutations in EMD may indicate a limb-girdle muscular dystrophy phenotype. Identification of emerin deficiency among patients with limb-girdle muscular dystrophy is essential to prevent cardiac catastrophe.

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Year:  2007        PMID: 17620497     DOI: 10.1001/archneur.64.7.1038

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  13 in total

Review 1.  Lamin-binding Proteins.

Authors:  Katherine L Wilson; Roland Foisner
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-02-17       Impact factor: 10.005

Review 2.  Lamina-associated polypeptide 1: protein interactions and tissue-selective functions.

Authors:  Ji-Yeon Shin; William T Dauer; Howard J Worman
Journal:  Semin Cell Dev Biol       Date:  2014-02-05       Impact factor: 7.727

Review 3.  The nuclear envelope: an intriguing focal point for neurogenetic disease.

Authors:  Howard J Worman; William T Dauer
Journal:  Neurotherapeutics       Date:  2014-10       Impact factor: 7.620

4.  Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1.

Authors:  Yuexia Wang; Ji-Yeon Shin; Koki Nakanishi; Shunichi Homma; Grace J Kim; Kurenai Tanji; Leroy C Joseph; John P Morrow; Colin L Stewart; Willian T Dauer; Howard J Worman
Journal:  Hum Mol Genet       Date:  2019-08-01       Impact factor: 6.150

5.  Tissue-specific defects are caused by loss of the Drosophila MAN1 LEM domain protein.

Authors:  Belinda S Pinto; Shameika R Wilmington; Emma E L Hornick; Lori L Wallrath; Pamela K Geyer
Journal:  Genetics       Date:  2008-08-24       Impact factor: 4.562

Review 6.  Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

Authors:  M N Astejada; K Goto; A Nagano; S Ura; S Noguchi; I Nonaka; I Nishino; Y K Hayashi
Journal:  Acta Myol       Date:  2007-12

Review 7.  The Pathogenesis and Therapies of Striated Muscle Laminopathies.

Authors:  Astrid Brull; Blanca Morales Rodriguez; Gisèle Bonne; Antoine Muchir; Anne T Bertrand
Journal:  Front Physiol       Date:  2018-10-30       Impact factor: 4.566

8.  Inhibition of extracellular signal-regulated kinase 1/2 signaling has beneficial effects on skeletal muscle in a mouse model of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutation.

Authors:  Antoine Muchir; Young Jin Kim; Sarah A Reilly; Wei Wu; Jason C Choi; Howard J Worman
Journal:  Skelet Muscle       Date:  2013-07-01       Impact factor: 4.912

Review 9.  The nuclear envelope LEM-domain protein emerin.

Authors:  Jason M Berk; Kathryn E Tifft; Katherine L Wilson
Journal:  Nucleus       Date:  2013-07-17       Impact factor: 4.197

10.  Expanding genotype/phenotype of neuromuscular diseases by comprehensive target capture/NGS.

Authors:  Xia Tian; Wen-Chen Liang; Yanming Feng; Jing Wang; Victor Wei Zhang; Chih-Hung Chou; Hsien-Da Huang; Ching Wan Lam; Ya-Yun Hsu; Thy-Sheng Lin; Wan-Tzu Chen; Lee-Jun Wong; Yuh-Jyh Jong
Journal:  Neurol Genet       Date:  2015-08-13
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