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1,100 Possible Causes for Proximal Muscle Weakness

  • Childhood Dermatomyositis

    Abstract A 62-year-old woman presented to the emergency department with malaise, lethargy and proximal muscle weakness. She had a similar presentation in childhood.[ncbi.nlm.nih.gov] Typical MRI and muscle biopsy changes were rated by all to be the most useful clinically relevant diagnostic criteria after proximal muscle weakness, characteristic skin rash[ncbi.nlm.nih.gov] They depend on the use of five diagnostic criteria: characteristic skin rash, proximal muscle weakness, raised muscle enzymes, myopathic changes on the electromyogram (EMG[rheumatology.oxfordjournals.org]

  • Polymyositis

    From Wikidata Jump to navigation Jump to search rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes edit[wikidata.org] This report highlights the case of a 30-year-old male who had severe myalgia and proximal muscle weakness.[ncbi.nlm.nih.gov] English polymyositis rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes PM Statements Identifiers Sitelinks[wikidata.org]

  • Dermatomyositis

    Later she developed progressive, symmetrical proximal muscle weakness.[ncbi.nlm.nih.gov] The prevailing clinical manifestations are intense erythema, typically around the eyes and dorsum of the hands, accompanied by proximal muscle weakness.[ncbi.nlm.nih.gov] It is characterized clinically by progressive symmetrical proximal muscle weakness and a characteristic rash.[ncbi.nlm.nih.gov]

  • Limb-Girdle Muscular Dystrophy

    Progressive proximal muscle weakness began again at age 8 years. Serum CK was 14,910 IU/L. She was wheelchair-bound by age 12.[ncbi.nlm.nih.gov] Moreover, polymyositis (PM) is manifested as symmetrical proximal muscle weakness of the four limbs, accompanied by an increased level of serum CK.[ncbi.nlm.nih.gov] Abstract The limb girdle muscular dystrophies are a heterogeneous group of conditions characterized by proximal muscle weakness and disease onset ranging from infancy to adulthood[ncbi.nlm.nih.gov]

  • Oculopharyngeal Muscular Dystrophy

    We describe a 70-year-old Italian woman with an adult-onset ptosis, mild dysphagia and proximal muscle weakness belonging to a family segregating OPMD according to an autosomal[ncbi.nlm.nih.gov] muscle weakness.[ncbi.nlm.nih.gov] In the presence of a positive family history and late-onset ptosis, dysphagia, and proximal muscle weakness (its cardinal features), we suggest that PABPN1 gene analysis should[ncbi.nlm.nih.gov]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2Q

    Autosomal recessive limb-girdle muscular dystrophy-17 is characterized by early childhood onset of proximal muscle weakness and atrophy without skin involvement.[ncbi.nlm.nih.gov] Muscle weakness may spread from the proximal muscles to affect distal muscles.[rarediseases.org] LGMD 2A (calpain 3) Childhood (8-15) There is mainly proximal muscle weakness. There is slow progression.[patient.info]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2J

    Muscle weakness may spread from the proximal muscles to affect distal muscles.[rarediseases.org] LGMD 2A (calpain 3) Childhood (8-15) There is mainly proximal muscle weakness. There is slow progression.[patient.info] Remember they will also have progressive proximal muscle weakness , as in polymyositis.[lecturio.com]

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1C

    Muscle weakness may spread from the proximal muscles to affect distal muscles.[rarediseases.org] […] and distal muscle weakness [ 3 ] Telethonin LGMD 2H Onset 1st to 3rd decade, proximal muscle weakness TRIM 32 gene LGMD 2I Onset 1 st to 3 rd decade.[jcdr.net] LGMD 2A (calpain 3) Childhood (8-15) There is mainly proximal muscle weakness. There is slow progression.[patient.info]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2T

    Muscle weakness may spread from the proximal muscles to affect distal muscles.[rarediseases.org] LGMD 2A (calpain 3) Childhood (8-15) There is mainly proximal muscle weakness. There is slow progression.[patient.info] Remember they will also have progressive proximal muscle weakness , as in polymyositis.[lecturio.com]

  • Multicore Myopathy

    Abstract Multicore myopathy, classified with the benign congenital myopathies, is manifest clinically as proximal muscle weakness, hypotonia, and delayed motor development[ncbi.nlm.nih.gov] It is marked by hypotonia and proximal muscle weakness.[kmle.co.kr] muscle weakness ; Ptosis ; Pulmonary hypoplasia ; Recurrent respiratory infections ; Respiratory insufficiency ; Scoliosis ; Skeletal muscle atrophy ; Type 1 and type 2 muscle[mousephenotype.org]

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