Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emery-dreifuss muscular dystrophy

Dropped head syndrome can be seen in many neuromuscular diseases. However, there are very few diseases in which neck extensors are weak among neuromuscular diseases. A 7 years old boy who had weakness of the neck extensor muscles, creatinine kinase elevation and dystrophy findings in biopsy followed up with the preliminary diagnosis of muscular dystrophy is presented. We detected p.N456K (c.1368C> A) heterozygote mutation by the gene sequencing in the Lamin A/C assocıated (LMNA) gene. This mutation was previously reported as Emery-Dreifuss muscular dystrophy.

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1.Reed UC. Congenital muscular dystrophy. Part 1: a review of phenotypical and diagnostic aspects. Arq Neuropsiquiatr 2009: 67; 144-168.

2.D’Amico A, Haliloglu G, Richard P, et al. Two patients with ‘Dropped head syndrome’ due to mutations in LMNA or SEPN1 genes. Neuromuscul Disord 2005; 15: 521-524.

3.Quijano-Roy S, Mbieleu B, Bönnemann C, et al. De novo LMNA mutations cause a new form of congenital muscular dystrophy. Ann Neurol 2008; 64: 177-186.

4.Jacob KN, Garg A. Laminopathies: multisystem dystrophy syndromes. Mol Genet Metab 2006; 87: 289-302.

5.Chemla JC, Kanter RJ, Carboni MP, Smith EC. Two children with ‘‘dropped head’’ syndrome due to lamin A/C mutations. Muscle Nerve 2010; 42: 839-841.

6.Karaoglu P, Quizon N, Pergande M, et al. Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA. Brain Dev 2017; 39: 361-364.

7.Pasqualin LMA, Reed UC , Costa TVMM, et al. Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohort. Pediatr Neurol 2014; 50: 400-406.

8.Ishiyama A, Iida A, Hayashi S, et al. A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy. Hum Genome Var 2018; 5: 19.

9.Bonne G, Mercuri E, Muchir A, et al. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Ann Neurol 2000; 48: 170-180.

10.Bonne G, Ben Yaou R, Beroud C, et al. 108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands. Neuromuscul Disord 2003; 13: 508-515.

11.Bonati U, Bechtel N, Heinimann K, et al. Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA gene. Neuromuscul Disord 2014; 24: 529-532.
Turkish Journal of Pediatrics-Cover
  • ISSN: 0041-4301
  • Yayın Aralığı: Yılda 6 Sayı
  • Başlangıç: 1958
  • Yayıncı: Hacettepe Üniversitesi Çocuk Sağlığı Enstitüsü Müdürlüğü
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