MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients

C Fiorillo, G Astrea, M. Savarese, D Cassandrini, G Brisca, F Trucco, M Pedemonte, R Trovato, L Ruggiero, Liliana Vercelli, A D'Amico, G Tasca, M. Pane, Marina Fanin, L Bello, P Broda, Olimpia1 Musumeci, C. Rodolico, S Messina, G L VitaMaria Sframeli, S Gibertini, L Morandi, M Mora, L Maggi, A. Petrucci, R. Massa, M. Grandis, A Toscano, E. Pegoraro, E. Mercuri, E Bertini, T. Mongini, L Santoro, V. Nigro, C Minetti, F M Santorelli, C Bruno, Italian Network on Congenital Myopathies

Research output: Contribution to journalArticle

Abstract

BACKGROUND: Myosin heavy chain 7 (MYH7)-related myopathies are emerging as an important group of muscle diseases of childhood and adulthood, with variable clinical and histopathological expression depending on the type and location of the mutation. Mutations in the head and neck domains are a well-established cause of hypertrophic cardiomyopathy whereas mutation in the distal regions have been associated with a range of skeletal myopathies with or without cardiac involvement, including Laing distal myopathy and Myosin storage myopathy. Recently the spectrum of clinical phenotypes associated with mutations in MYH7 has increased, blurring this scheme and adding further phenotypes to the list. A broader disease spectrum could lead to misdiagnosis of different congenital myopathies, neurogenic atrophy and other neuromuscular conditions.

RESULTS: As a result of a multicenter Italian study we collected clinical, histopathological and imaging data from a population of 21 cases from 15 families, carrying reported or novel mutations in MYH7. Patients displayed a variable phenotype including atypical pictures, as dropped head and bent spine, which cannot be classified in previously described groups. Half of the patients showed congenital or early infantile weakness with predominant distal weakness. Conversely, patients with later onset present prevalent proximal weakness. Seven patients were also affected by cardiomyopathy mostly in the form of non-compacted left ventricle. Muscle biopsy was consistent with minicores myopathy in numerous cases. Muscle MRI was meaningful in delineating a shared pattern of selective involvement of tibialis anterior muscles, with relative sparing of quadriceps.

CONCLUSION: This work adds to the genotype-phenotype correlation of MYH7-relatedmyopathies confirming the complexity of the disorder.

Original languageEnglish
Pages (from-to)91
JournalOrphanet Journal of Rare Diseases
Volume11
Issue number1
DOIs
Publication statusPublished - Jul 7 2016

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Myosin Heavy Chains
Muscular Diseases
Mutation
Muscles
Phenotype
Distal Myopathies
Head
Myotonia Congenita
Hypertrophic Cardiomyopathy
Genetic Association Studies
Diagnostic Errors
Cardiomyopathies
Multicenter Studies
Heart Ventricles
Atrophy
Neck
Biopsy
Population

Keywords

  • Journal Article

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MYH7-related myopathies : clinical, histopathological and imaging findings in a cohort of Italian patients. / Fiorillo, C; Astrea, G; Savarese, M.; Cassandrini, D; Brisca, G; Trucco, F; Pedemonte, M; Trovato, R; Ruggiero, L; Vercelli, Liliana; D'Amico, A; Tasca, G; Pane, M.; Fanin, Marina; Bello, L; Broda, P; Musumeci, Olimpia1; Rodolico, C.; Messina, S; Vita, G L; Sframeli, Maria; Gibertini, S; Morandi, L; Mora, M; Maggi, L; Petrucci, A.; Massa, R.; Grandis, M.; Toscano, A; Pegoraro, E.; Mercuri, E.; Bertini, E; Mongini, T.; Santoro, L; Nigro, V.; Minetti, C; Santorelli, F M; Bruno, C; Italian Network on Congenital Myopathies.

In: Orphanet Journal of Rare Diseases, Vol. 11, No. 1, 07.07.2016, p. 91.

Research output: Contribution to journalArticle

Fiorillo, C, Astrea, G, Savarese, M, Cassandrini, D, Brisca, G, Trucco, F, Pedemonte, M, Trovato, R, Ruggiero, L, Vercelli, L, D'Amico, A, Tasca, G, Pane, M, Fanin, M, Bello, L, Broda, P, Musumeci, O, Rodolico, C, Messina, S, Vita, GL, Sframeli, M, Gibertini, S, Morandi, L, Mora, M, Maggi, L, Petrucci, A, Massa, R, Grandis, M, Toscano, A, Pegoraro, E, Mercuri, E, Bertini, E, Mongini, T, Santoro, L, Nigro, V, Minetti, C, Santorelli, FM, Bruno, C & Italian Network on Congenital Myopathies 2016, 'MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients', Orphanet Journal of Rare Diseases, vol. 11, no. 1, pp. 91. https://doi.org/10.1186/s13023-016-0476-1
Fiorillo, C ; Astrea, G ; Savarese, M. ; Cassandrini, D ; Brisca, G ; Trucco, F ; Pedemonte, M ; Trovato, R ; Ruggiero, L ; Vercelli, Liliana ; D'Amico, A ; Tasca, G ; Pane, M. ; Fanin, Marina ; Bello, L ; Broda, P ; Musumeci, Olimpia1 ; Rodolico, C. ; Messina, S ; Vita, G L ; Sframeli, Maria ; Gibertini, S ; Morandi, L ; Mora, M ; Maggi, L ; Petrucci, A. ; Massa, R. ; Grandis, M. ; Toscano, A ; Pegoraro, E. ; Mercuri, E. ; Bertini, E ; Mongini, T. ; Santoro, L ; Nigro, V. ; Minetti, C ; Santorelli, F M ; Bruno, C ; Italian Network on Congenital Myopathies. / MYH7-related myopathies : clinical, histopathological and imaging findings in a cohort of Italian patients. In: Orphanet Journal of Rare Diseases. 2016 ; Vol. 11, No. 1. pp. 91.
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T1 - MYH7-related myopathies

T2 - clinical, histopathological and imaging findings in a cohort of Italian patients

AU - Fiorillo, C

AU - Astrea, G

AU - Savarese, M.

AU - Cassandrini, D

AU - Brisca, G

AU - Trucco, F

AU - Pedemonte, M

AU - Trovato, R

AU - Ruggiero, L

AU - Vercelli, Liliana

AU - D'Amico, A

AU - Tasca, G

AU - Pane, M.

AU - Fanin, Marina

AU - Bello, L

AU - Broda, P

AU - Musumeci, Olimpia1

AU - Rodolico, C.

AU - Messina, S

AU - Vita, G L

AU - Sframeli, Maria

AU - Gibertini, S

AU - Morandi, L

AU - Mora, M

AU - Maggi, L

AU - Petrucci, A.

AU - Massa, R.

AU - Grandis, M.

AU - Toscano, A

AU - Pegoraro, E.

AU - Mercuri, E.

AU - Bertini, E

AU - Mongini, T.

AU - Santoro, L

AU - Nigro, V.

AU - Minetti, C

AU - Santorelli, F M

AU - Bruno, C

AU - Italian Network on Congenital Myopathies

PY - 2016/7/7

Y1 - 2016/7/7

N2 - BACKGROUND: Myosin heavy chain 7 (MYH7)-related myopathies are emerging as an important group of muscle diseases of childhood and adulthood, with variable clinical and histopathological expression depending on the type and location of the mutation. Mutations in the head and neck domains are a well-established cause of hypertrophic cardiomyopathy whereas mutation in the distal regions have been associated with a range of skeletal myopathies with or without cardiac involvement, including Laing distal myopathy and Myosin storage myopathy. Recently the spectrum of clinical phenotypes associated with mutations in MYH7 has increased, blurring this scheme and adding further phenotypes to the list. A broader disease spectrum could lead to misdiagnosis of different congenital myopathies, neurogenic atrophy and other neuromuscular conditions.RESULTS: As a result of a multicenter Italian study we collected clinical, histopathological and imaging data from a population of 21 cases from 15 families, carrying reported or novel mutations in MYH7. Patients displayed a variable phenotype including atypical pictures, as dropped head and bent spine, which cannot be classified in previously described groups. Half of the patients showed congenital or early infantile weakness with predominant distal weakness. Conversely, patients with later onset present prevalent proximal weakness. Seven patients were also affected by cardiomyopathy mostly in the form of non-compacted left ventricle. Muscle biopsy was consistent with minicores myopathy in numerous cases. Muscle MRI was meaningful in delineating a shared pattern of selective involvement of tibialis anterior muscles, with relative sparing of quadriceps.CONCLUSION: This work adds to the genotype-phenotype correlation of MYH7-relatedmyopathies confirming the complexity of the disorder.

AB - BACKGROUND: Myosin heavy chain 7 (MYH7)-related myopathies are emerging as an important group of muscle diseases of childhood and adulthood, with variable clinical and histopathological expression depending on the type and location of the mutation. Mutations in the head and neck domains are a well-established cause of hypertrophic cardiomyopathy whereas mutation in the distal regions have been associated with a range of skeletal myopathies with or without cardiac involvement, including Laing distal myopathy and Myosin storage myopathy. Recently the spectrum of clinical phenotypes associated with mutations in MYH7 has increased, blurring this scheme and adding further phenotypes to the list. A broader disease spectrum could lead to misdiagnosis of different congenital myopathies, neurogenic atrophy and other neuromuscular conditions.RESULTS: As a result of a multicenter Italian study we collected clinical, histopathological and imaging data from a population of 21 cases from 15 families, carrying reported or novel mutations in MYH7. Patients displayed a variable phenotype including atypical pictures, as dropped head and bent spine, which cannot be classified in previously described groups. Half of the patients showed congenital or early infantile weakness with predominant distal weakness. Conversely, patients with later onset present prevalent proximal weakness. Seven patients were also affected by cardiomyopathy mostly in the form of non-compacted left ventricle. Muscle biopsy was consistent with minicores myopathy in numerous cases. Muscle MRI was meaningful in delineating a shared pattern of selective involvement of tibialis anterior muscles, with relative sparing of quadriceps.CONCLUSION: This work adds to the genotype-phenotype correlation of MYH7-relatedmyopathies confirming the complexity of the disorder.

KW - Journal Article

U2 - 10.1186/s13023-016-0476-1

DO - 10.1186/s13023-016-0476-1

M3 - Article

C2 - 27387980

VL - 11

SP - 91

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

SN - 1750-1172

IS - 1

ER -