Open AccessProgression to Loss of Ambulation Among Patients with Autosomal Recessive Limb-girdle Muscular Dystrophy: A Systematic Review
Author(s) -
I. Filipovic Audhya,
Antoinette Cheung,
Shelagh M. Szabo,
Emma Flint,
Conrad C. Weihl,
Katherine Gooch
Publication year - 2022
Publication title -
journal of neuromuscular diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 23
eISSN - 2214-3602
pISSN - 2214-3599
DOI - 10.3233/jnd-210771
Subject(s) - medicine , age of onset , pediatrics , limb girdle muscular dystrophy , early childhood , disease , muscular dystrophy , myopathy , young adult , mutation , psychology , developmental psychology , biochemistry , chemistry , gene
BackgroundThe impact of age at autosomal recessive limb girdle muscular dystrophy (LGMDR) onset on progression to loss of ambulation (LOA) has not been well established, particularly by subtype.