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17 Possible Causes for Bilateral Arm Weakness, Facial Muscle Weakness and Progressive Atrophy, Muscular Atrophy

  • Amyotrophic Lateral Sclerosis

    Here, we report a patient who presented with progressive left arm weakness and was found to have bilateral MRI plexus abnormalities.[ncbi.nlm.nih.gov] The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Multifocal Motor Neuropathy

    Abstract Multifocal motor neuropathy (MMN) and progressive muscular atrophy (PMA) are associated with IgM monoclonal gammopathy or the presence IgM anti-GM1-antibodies.[ncbi.nlm.nih.gov] In the first patient the symptoms were slowly progressive with bulbar muscle impairment, generalized weakness, muscular atrophy with cramps and fasciculations.[moh-it.pure.elsevier.com] Monoclonal gammopathy was determined by immunoelectrophoresis and immunofixation in serum from 445 patients with ALS, 158 patients with progressive muscular atrophy (PMA),[ncbi.nlm.nih.gov]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    […] restricted to one half ofthe body Bulbar/pseudobulbar palsy 19.  1-2% -Weakness of respiratory group of muscles 10% - Bilateral upper limb weakness and wasting, flail[slideshare.net] […] are not associated with a defect in the SMN1 gene on chromosome 5q X-linked spinal muscular atrophy X-linked spinal muscular atrophy is seen only among males![amboss.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Spinal Muscular Atrophy with Respiratory Distress Type 1

    […] muscle weakness (Usually upper arms & legs more so than hands and feet) preceded by an asymptomatic period (all but most severe type 0) Flattening of the chest wall when[en.wikipedia.org] Homepage Rare diseases Search Search for a rare disease Spinal muscular atrophy with respiratory distress type 1 Disease definition Spinal muscular atrophy with respiratory[orpha.net] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Lambert Eaton Myasthenic Syndrome

    Spinal muscular atrophy.[patient.info] MuSK MG should be considered if there is facial or tongue weakness with atrophy, or weakness that predominates in neck or shoulder muscles.[docksci.com] The type 2 fiber atrophy, found on the histochemical study of the brachial biceps muscular biopsy of both patients, is an non-specified finding.[scielo.br]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2R

    In a family showing a missense Ala337Pro mutation, disease started with gait disturbance and bilateral weakness in the lower limbs.[doi.org] ATROPHIES & MOTOR NEURON DISEASES Spinal muscular atrophy, type I-IV (SMN1) Spinal muscular atrophy, autosomal dominant, proximal, adult-onset (VAPB) Spinal muscular atrophy[meduniwien.ac.at] Specifically, LGMD2B is a slowly progressive disease that causes muscle weakness and wasting ( atrophy ) of the pelvic muscles and muscles of the shoulder girdle. 0003236[rarediseases.info.nih.gov]

  • Distal Myopathy Type 3

    weakness H/o HTN , dyslipidaemia DM Weakness of the involved arm Head CT Normal Normal Neuropathic GBS [27] 18 350 Proximal Ascending paralysis Precedes a gastrointestinal[wikidoc.org] Marked facial weakness is observed in these patients with congenital myopathies. [2] Spinal Muscular Atrophy Distal spinal muscular atrophy is an autosomal recessive infantile[explainmedicine.com] The following features are however constantly present: atrophy of the intrinsic hand muscles, facial muscle involvement, myotonia and dystrophic changes in nonmuscular tissue[neuroweb.us]

  • Facioscapulohumeral Muscular Dystrophy

    The patient had moderate facial weakness and marked winging and high-riding of the scapulae with prominent pectoral and proximal arm muscle atrophy and weakness.[ncbi.nlm.nih.gov] Muscular atrophy in the face, shoulder girdle and upper arms was observed from the age of 4 years.[ncbi.nlm.nih.gov] Facioscapulohumeral muscular dystrophy is an autosomal-dominant, slowly progressive myopathy that involves facial, shoulder, and upper arm muscles.[ncbi.nlm.nih.gov]

  • Fingerprint Body Myopathy

    B Atrophy of the proximal arm muscles, neck muscles, and weakness of the facial muscles. C Bilateral hand wasting Fig. 20. Nemaline myopathy.[rrnursingschool.biz] He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy.[books.google.com] Within few years the disease progressed to generalized muscle weakness and atrophy, ptosis, ophthalmoplegia externa and areflexia.[scipers.com]

  • Spastic Ataxia with Congenital Miosis

    […] trigeminal neuralgia and weakness of arm What is the most common site (30%) of hypertensive hemorrhage?[quizlet.com] atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Pure[se-atlas.de] - initial complaint of overall leg weakness affecting stair climbing and walking - weakness starts in the thighs and ascends to arms in days - Pain in 30% - bilateral sciatica[flashcardmachine.com]

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