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- Disease Information
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Disease Information for Erb's Muscular Dystrophy/Limb Girdle MD
- Clinical Manifestations
- Signs & Symptoms
- Adolescent
- Arm/shoulder weakness (symptom)
- Bilateral Shoulder Muscle pain/Weakness
- Muscle Atrophy
- Muscle weakness
- Pelvic/limb girdle weakness/bilateral
- Proximal muscle weakness
- Proximal symmetrical muscle weakness
- Shoulder/limb girdle weakness/bilateral
- Unable to stand up from sitting position
- Weak/Weak as a kitten (symptom)
- Weakness, arms, bilateral
- Winging of scapula
- Hyporeflexia/DTRs decreased
- Limb weakness/signs
- Waddling Trendelenberg Gait
- Weakness/Diffuse motor loss
- Child won't walk
- Balance problems
- Difficulty raising arms
- Enervated/extreme acute fatigue
- Falling
- Muscle Wasting/Diffuse
- Weakness
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Course/Life-span decreased
- Course/Progressive
- Course/Progressive/slowly chronic illness
- Onset/Young adult
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Young Adult
- Family History
- Family history/Muscle disease/Muscular dystrophy
- Sex & Age Groups
- Population/Adolescent
- Population/Adult ('twenties')
- Population/Adult/all
- Population/Child
- Population/Children/all
- Population/Male
- Population/Pre-teen
- Population/Twenties-Adult/female
- Population/Twenties-Adult/male
- Population/Young adult
- Laboratory Tests
- Abnormal Lab Findings - Increased
- Aldolase, serum (Lab)
- Diagnostic Test Results
- Pathology
- BX/Muscle Biopsy Abnormal
- BX/Muscle biopsy/Fiber atrophy
- BX/Muscle biopsy/Increased interstitial tissue
- BX/Muscle biopsy/Increased sarcolemma nuclei
- BX/Muscle Biopsy/Loss striation/swelling
- BX/Muscle biopsy/muscle fiber degeneration
- Electrodiagnosis
- EMG/Abnormal findings
- EMG/Muscular Dystrophic signs
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Erbs Muscular Dystrophy/Limb Girdle MD
- Muscular dystrophy
- Ineffective Cough or Reflex
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Extremities/Digits/Hand feet disorder (category)
- CLASS/Muscle disorder (ex)
- CLASS/Muscle/tendon/extremities (category)
- CLASS/Striated muscle disorder (ex)
- Pathophysiology
- Pathophysiology/Sporadic/hereditary/process
- Pathophysiology/Maternal Chromosome mutation
- Process
- PROCESS/Atrophic disorders (ex)
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Autosomal recessive disorder (ex)
- PROCESS/Degenerative/necrosis disorder (category)
- PROCESS/Developmental/delayed expression disorder (ex)
- PROCESS/Dystrophic disorder (ex)
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Use/Age/atrophic disorder (category)
- PROCESS/Muscular dystrophy disorder (ex)
- Synonyms
- Synonym
- dystrophy muscular limb girdle, Leyden Mobius muscular dystrophy, Leyden Möbius muscular dystrophy, Limb Girdle Muscular Dystrophies, Limb Girdle Muscular Dystrophy, Limb girdle muscular dystrophy (disorder), limb girdle muscular dystrophy (LGMD), limb girdle muscular weakness and atrophy, limb girdle syndrome, limb girdle syndrome (LGS), Muscular Dystrophies Limb Girdle, Muscular Dystrophy Limb Girdle, MUSCULAR DYSTROPHY LIMB GIRDLE TYPE, myopathic limb girdle syndrome, Synonym/Erb Juvenile Muscular dystrophy, Synonym/Limb Girdle Muscular dystrophy/Erb's, Synonym/Muscular Dystrophy/Limb girdle type, Synonym/Scapulohumeral muscular dystrophy/Erb's
- Treatment
- Other Treatments
- TX/Physical therapy
- Definition
-
Muscular Dystrophy, Limb Girdle; Erb Muscular Dystrophy; LGMD; Leyden-Moebius Muscular Dystrophy; Pelvofemoral Muscular Dystrophy; Proximal Muscular Dystrophy; Limb-Girdle Muscular Dystrophy is a group of inherited, progressive disorders that are characterized by weakness and wasting (atrophy) of muscles of the hip and shoulder areas; Several different forms of the disorder have been identified that are caused by abnormal changes (mutations) of certain genes; Of these disease subtypes, at least eight have autosomal recessive inheritance and at least three are transmitted as an autosomal dominant trait; In most individuals with Limb-Girdle Muscular Dystrophy, associated symptoms and findings become apparent during childhood; However, less commonly, symptom onset may begin during adolescence or adulthood; Muscle weakness may spread from the lower limbs to the upper limbs or vice versa; Although the disorder typically progresses slowly, some affected individuals experience rapid disease progression---------[NORD]--------------------
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- External Links Related to Erb's Muscular Dystrophy/Limb Girdle MD
- Wikipedia
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- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)