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Limb-girdle muscular dystrophy (LGMD) is a diverse group of disorders with many subtypes categorized by disease gene and inheritance. LGMD usually manifests in the proximal muscles around the hips and shoulders.
Limb-girdle muscular dystrophy (LGMD) is a group of rare muscular dystrophies that cause muscle weakness in your shoulders, upper arms, hips and upper legs. There are several different subtypes based on which gene has a mutation.
Limb-girdle muscular dystrophy is a term for a group of diseases that cause weakness and wasting of the muscles in the arms and legs. Explore symptoms, inheritance, genetics of this condition.
Limb-girdle muscular dystrophy (LGMD) is a general term used to describe a group of diseases that causes wasting and weakness in the muscles of the arms and legs, particularly in the muscles around the shoulders and hips (the limb girdles).
Limb–girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics. [7] It is characterised by progressive muscle wasting which affects predominantly hip and shoulder muscles. [8] LGMD usually has an autosomal pattern of inheritance.
Limb-girdle muscular dystrophy is a group of disorders which affect the voluntary muscles around the hips and shoulders. Males and females are affected in equal numbers. Most forms of limb girdle muscular dystrophy are inherited in an autosomal recessive manner.
The Limb Girdle muscular dystrophies (LGMD) comprise at least a dozen different specific entities. Each of these distinct disorders is in itself rare. Patients with LGMD usually begin to have symptoms in adolescence or early adulthood, however, some forms of LGMD are more severe with symptoms beginning in childhood.
Limb girdle muscular dystrophy (LGMD) is a group of conditions that causes muscle weakness and wasting. Learn about symptoms, causes, treatments, and more.
Limb girdle muscular dystrophies (LGMDs) are rare conditions and they present differently in people, even within the same family, with regard to age of onset, areas of muscle weakness, heart and respiratory involvement, rate of progression and severity.
Limb-girdle muscular dystrophies are a large group of genetic diseases in which there is muscle weakness and wasting (muscular dystrophy). In most cases, both parents must pass on the non-working (defective) gene for a child to have the disease (autosomal recessive inheritance).