Expanding the Importance of Hmerf Titinopathy: New Mutations and Clinical Aspects Publisher Pubmed



Palmio J¹ ; Leonardlouis S² ; Sacconi S³ ; Savarese M⁴ ; Penttila S¹ ; Semmler AL^{5, 6} ; Kress W⁷ ; Mozaffar T⁸ ; Lai T⁸ ; Stojkovic T⁹ ; Berardo A¹⁰ ; Reisin R¹⁰ ; Attarian S¹¹ ; Urtizberea A¹² Show All Authors
Source: Journal of Neurology Published:2019

Abstract

Objective: Hereditary myopathy with early respiratory failure (HMERF) is caused by titin A-band mutations in exon 344 and considered quite rare. Respiratory insufficiency is an early symptom. A collection of families and patients with muscle disease suggestive of HMERF was clinically and genetically studied. Methods: Altogether 12 new families with 19 affected patients and diverse nationalities were studied. Most of the patients were investigated using targeted next-generation sequencing; Sanger sequencing was applied in some of the patients and available family members. Histological data and muscle MRI findings were evaluated. Results: Three families had several family members studied while the rest were single patients. Most patients had distal and proximal muscle weakness together with respiratory insufficiency. Five heterozygous TTN A-band mutations were identified of which two were novel. Also with the novel mutations the muscle pathology and imaging findings were compatible with the previous reports of HMERF. Conclusions: Our collection of 12 new families expands mutational spectrum with two new mutations identified. HMERF is not that rare and can be found worldwide, but maybe underdiagnosed. Diagnostic process seems to be complex as this study shows with mostly single patients without clear dominant family history. © 2019, The Author(s).