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255 Possible Causes for Amyotrophic Lateral Sclerosis, primarily in the legs, severe muscle wasting

Did you mean: Amyotrophic Lateral Sclerosis, primarily in the legs, severe, muscle wasting

  • Spinal Muscular Atrophy

    The latter is the only drug with proven, albeit modest, efficacy in the treatment of amyotrophic lateral sclerosis.[ncbi.nlm.nih.gov] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org] […] diagnosis of infants with congenital contractures and severe muscle weakness by wasting mainly confined to the upper limbs.[ncbi.nlm.nih.gov]

  • Adult Spinal Muscular Atrophy

    […] spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[symptoma.com] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org] Society. 1993 Research Grants & Projects Plain Text Genetics in motor neuron disease Gene Science Research[researchmap.jp]

  • Spinal Muscular Atrophy Type 3

    SMA type IV is the least severe type of the disease where weakness and muscle wasting generally start in adulthood.[stemcellthailand.org] Neuron Disease 1st March 2017 Conditions : Motor Neuron Disease; Amyotrophic Lateral Sclerosis; Primary Lateral Sclerosis; Progressive Muscular Atrophy; Progressive Bulbar[treat-nmd.eu] This form affects primarily the muscles in the legs.[mda.org]

  • Spinal Muscular Atrophy Type 1

    atrophy type 1 with paradoxical breathing were placed on high-span PIP PEEP when sleeping from the point of diagnosis of spinal muscular atrophy.[ncbi.nlm.nih.gov] SMA is a motor neuron disease that affects the voluntary muscles that are used for activities such as crawling, walking, head and neck control, and swallowing.[smartspeechtherapy.com] This form affects primarily the muscles in the legs.[mda.org]

  • Muscular Atrophy

    Neuromyopathy associated ketosis should be considered in all patients with severe muscle wasting presenting with an elevated anion gap metabolic ketoacidosis.[ncbi.nlm.nih.gov] neuron disease G12.21 Amyotrophic lateral sclerosis G12.22 Progressive bulbar palsy G12.23 Primary lateral sclerosis G12.24 Familial motor neuron disease G12.25 Progressive[icd10data.com] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io] Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.[sydney.edu.au] This form affects primarily the muscles in the legs.[mda.org]

  • Progressive Bulbar Palsy

    […] term(s): Adult form spinal muscular atrophy Childhood form, type II spinal muscular atrophy Distal spinal muscular atrophy Juvenile form, type III spinal muscular atrophy[icd10coded.com] Motor Neuron Disease (or ‘amyotrophic lateral sclerosis’, ALS). ‘’Brain Damage, Brain Repair.’’[en.wikipedia.org] She has a little weakness in her left leg and arm, but still has good use of them so far. She has also started having problems breathing at times.[inspire.com]

  • Amyotrophic Lateral Sclerosis

    Excluding lower motor neuron FA and FL cases, progressive muscular atrophy comprised 4% of the sample and had a prognosis similar to typical limb onset ALS.[ncbi.nlm.nih.gov] Medication in the last days of life for motor neuron disease/amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. 11, 562–564 (2010). 35.[doi.org] […] by often asymmetric and primarily distal LMN involvement in the lower limbs.[doi.org]

  • Monomelic Amyotrophy

    Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical[doi.org] Disorder progression tends to be slower in patients who are younger than 40 at onset, [ 8 ] [ 9 ] are mildly obese, [ 10 ] have disorder restricted primarily to one limb,[cinabrio.over-blog.es] Rev Neurol (Paris) 145: 163–8 Medline, Google Scholar Hirayama K ( 2000 ) Juvenile muscular atrophy of distal upper extremity (Hirayama Disease).[doi.org]

  • Distal Hereditary Motor Neuropathy

    Neurological examination revealed a symmetrical severe muscle wasting and weakness in distal lower and upper limbs, with claw hands, footdrop with equinovarus deformity and[ncbi.nlm.nih.gov] lateral sclerosis and amyotrophic lateral sclerosis‑frontotemporal dementia.[ncbi.nlm.nih.gov] It results in muscle weakness and affects movement, primarily in the legs.[ghr.nlm.nih.gov]

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