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Pane, M; Messina, S; Vasco, G; Foley, A.R; Morandi, L; Pegoraro, E; Mongini, T; D’Amico, A; Bianco, F; Lombardo, M.E; Scalise, R; Bruno, C; Berardinelli, A; Pini, A; Moroni, I; Mora, M; Toscano, A; Moggio, M; Comi, G; Santorelli, F.M; Bertini, E; Muntoni, F; Mercuri, E
Neuromuscular disorders, 08/2012, Letnik: 22, Številka: 8Journal Article
Abstract The aim of this retrospective study was to assess respiratory and cardiac function in a large cohort of patients with congenital muscular dystrophies (CMD) with reduced glycosylation of alphadystroglycan (α-DG). Thirteen of the 115 patients included in the study died between the age of 1 month and 20 years. The age at last follow up of the surviving 102 ranged between 1 year and 68 years (median: 9.3 years). Cardiac involvement was found in 7 of the 115 (6%), 5 with dilated cardiomyopathy, 1 cardiac conductions defects and 1 mitral regurgitation. Respiratory function was impaired in 14 (12%). Ten of the 14 required non invasive nocturnal respiratory support, while the other four required invasive ventilation. Cardiac or respiratory involvement was found in patients with mutations in FKRP , POMT1 , POMT2 . All of the patients in whom mutation in POMGnT1 were identified had normal cardiac and respiratory function.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Vir: Osebne bibliografije
in: SICRIS
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