A multicenter, retrospective medical record review of X‐linked myotubular myopathy: The recensus study
Year: 2017
Type: article
Study design: Observational Study
Abstract: INTRODUCTION: X-linked myotubular myopathy (XLMTM), characterized by severe hypotonia, weakness, respiratory distress, and early mortality, is rare and natural history studies are few. METHODS: RECENSUS is a multicenter chart review of male XLMTM patients characterizing disease burden and unmet medical needs. Data were collected between September 2014 and June 2016. RESULTS: Analysis included 112 patients at six clinical sites. Most recent patient age recorded was ≤18 months for 40 patients and >18 months for 72 patients. Mean (SD) age at diagnosis was 3.7 (3.7) months and 54.3 (77.1) months, respectively. Mortality was 44% (64% ≤18 months; 32% >18 months). Premature delivery occurred in 34/110 (31%) births. Nearly all patients (90%) required respiratory support at birth. In the first year of life, patients underwent an average of 3.7 surgeries and spent 35% of the year in the hospital. DISCUSSION: XLMTM is associated with high mortality, disease burden, and healthcare utilization. Muscle Nerve 57: 550-560, 2018.
Source: Muscle & Nerve
DOI: 10.1002/mus.26018
Institutions: Boston Children's Hospital, Harvard University, Manton Center for Orphan Disease Research, University of Florida Health, University of Florida, Cure CMD, Royal Manchester Children's Hospital, Audentes Therapeutics (United States), Lurie Children's Hospital, Statistics Collaborative, Children's Hospital Colorado, Children's Hospital of Philadelphia, University of Pennsylvania
Language: English
Subfield: Genetics (clinical)
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,610
OpenAlex ID: W2769220832
