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155 Possible Causes for Global Muscle Weakness

  • Autosomal Recessive Spastic Paraplegia Type 18

    About the Editors Professor Anthony Schapira is Professor of Neurological Science and Head of the Department of Clinical Neuroscience at the UCL Institute of Neurology, London, UK and Chairman of Clinical Neurosciences Specialties. Zbigniew Wszolek , MD, is Professor of Neurology in the Department of Neurology,[…][]

  • Ganglioneuroma

    CASE DESCRIPTION: A 40-year-old man presented with a right sciatica episode accompanied by global muscle weakness and tingling pain.[]

  • Odontomatosis - Aortae Esophagus Stenosis Syndrome

    […] cramps Intellectual disability Seizures Global developmental delay Generalized hypotonia Pica Ataxia Muscle weakness Spasticity Peripheral neuropathy Dysarthria Optic atrophy[] […] horn cell morphology Therapeutic abortion Internuclear ophthalmoplegia GM2-ganglioside accumulation Zebra bodies Autosomal dominant inheritance Neoplasm Memory impairment Muscle[]

  • Amyotrophic Lateral Sclerosis 5

    There was global muscle weakness and atrophy of the right leg, and mild muscle atrophy in the left leg.[] Over the subsequent 10 months, his weakness progressed quickly to involve proximal muscles of right lower limb, and then left leg.[]

  • Congenital Merosin-Positive Muscular Dystrophy

    The first patient, a 15-month-old boy with hypotonia, muscle weakness and global development delay, had moderate cerebellar atrophy and mild dilatation of the lateral ventricles[]

  • Congenital Muscular Dystrophy

    A 5 year-old boy exhibited global hypotonia with generalized muscle weakness from birth.[] Disease International Registry (CMDIR) Welcomes everyone with congenital or later onset muscle weakness (such as limb girdle muscular dystrophy) to participate .[] Core clinical phenotype included global developmental delay prominent in gross-motor and language domains, severe intellectual disability (ID), and/or muscle weakness in all[]

  • Ischemic Peripheral Neuropathy

    It can present with global muscle pain, weakness, and a warm hand with palpable pulses starting within the 1 st h after the creation of the AV fistula.[]

  • Pontocerebellar Hypoplasia Type 1B

    Objectives: Pontocerebellar hypoplasia with spinal muscular atrophy, also known as PCH1, is a group of autosomal recessive disorders characterized by generalized muscle weakness[] There is diffuse muscle weakness, progressive microcephaly, global developmental delay, and brainstem involvement.[] […] and global developmental delay commonly resulting in early death.[]

  • Autosomal Dominant Progressive External Ophthalmoplegia

    […] developmental delay ; Glucose intolerance ; Increased serum lactate ; Limb muscle weakness ; Multiple mitochondrial DNA deletions ; Myalgia ; Progressive ; Progressive external[] […] transaminase ; Elevated serum creatine phosphokinase ; Exercise intolerance ; Facial palsy ; Failure to thrive ; Gastroesophageal reflux ; Gastroparesis ; Generalized hypotonia ; Global[] […] neurological Phenotypes Adult onset ; Arrhythmia ; Autosomal dominant inheritance ; Cerebellar atrophy ; Cerebral visual impairment ; Constipation ; Cytochrome C oxidase-negative muscle[]

  • Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia

    weakness 59 32 frequent (33%) Frequent (79-30%) HP:0003324 10 hyperactive deep tendon reflexes 59 32 frequent (33%) Frequent (79-30%) HP:0006801 11 moderate global developmental[] 0002321 7 intellectual disability, moderate 59 32 frequent (33%) Frequent (79-30%) HP:0002342 8 poor speech 59 32 frequent (33%) Frequent (79-30%) HP:0002465 9 generalized muscle[]

Further symptoms