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87 Possible Causes for Atrophy of the Small Muscles in the Hand

  • Mitochondrial Membrane Protein-Associated Neurodegeneration

    Neurocase. 2016 Oct;22(5):476-483. Epub 2016 Nov 1. Author information 1 a Department of Neurology , University Hospitals Case Medical Center , Beachwood , OH , USA. 2 b Departments of Neurology and Psychiatry , University Hospitals Case Medical Center , 3619 Park East Drive, Beachwood , OH , USA. 3 c Department of[…][ncbi.nlm.nih.gov]

  • Distal Myopathy Type Tateyama

    Muscle atrophy may be restricted to the small muscles of the hands and feet.[malacards.org] Format Definition A disorder characterized by progressive muscular atrophy and muscle weakness beginning in the hands, the legs, or the feet.[uniprot.org] People with CAV3-related distal myopathy experience wasting ( atrophy ) and weakness of the small muscles in the hands and feet that generally become noticeable in adulthood[familydiagnosis.com]

  • Hereditary Areflexic Dystasia

    […] with slight atrophy of the small muscles of the hand, (6) decreased faradic and galvanic excitability of muscles, and (7) atypical tremor of the hands, made evident by tensing[jamanetwork.com] […] gait, (2) abnormalities of equilibrium which were evident on standing and more pronounced with eye closure, (3) areflexia, (4) clubfeet, (5) awkwardness and weakness of the hands[jamanetwork.com]

  • Distal Hereditary Motor Neuropathy

    small muscles of the hands. [3] Signs and symptoms Onset usually occurs within the first two decades of life, commonly in the teenage years or the twenties.[ipfs.io] Physical examination revealed atrophy and weakness of small hand muscles and mild atrophy and weakness of the lower limbs.[ncbi.nlm.nih.gov] It is allelic (i.e., caused by mutations on the same gene) with Charcot–Marie–Tooth disease and with Silver’s Syndrome, a disorder also characterized by small muscle atrophy[ipfs.io]

  • Distal Hereditary Motor Neuropathy Type Jerash

    small muscles of the hands. [3] Signs and symptoms [ edit ] Onset usually occurs within the first two decades of life, commonly in the teenage years or the twenties.[en.wikipedia.org] It is allelic (i.e., caused by mutations on the same gene) with Charcot–Marie–Tooth disease and with Silver’s Syndrome, a disorder also characterized by small muscle atrophy[en.wikipedia.org] Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance , weakness of the upper limbs that is progressive and symmetrical, and atrophy of the[en.wikipedia.org]

  • Distal Hereditary Motor Neuropathy Type 5

    small muscles of the hands. [3] Signs and symptoms [ edit ] Onset usually occurs within the first two decades of life, commonly in the teenage years or the twenties.[en.wikipedia.org] It is allelic (i.e., caused by mutations on the same gene) with Charcot–Marie–Tooth disease and with Silver’s Syndrome, a disorder also characterized by small muscle atrophy[en.wikipedia.org] Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance , weakness of the upper limbs that is progressive and symmetrical, and atrophy of the[en.wikipedia.org]

  • Ulnar Nerve Entrapment

    Progressively the problem goes on to produce weakness in the hand and atrophy of the small muscles in the hand. Diagnosis is confirmed by nerv conduction studies.[ukriversguidebook.co.uk] The hand muscles can become thinner (atrophy), so that the hand becomes "knuckly" and hollows develop between the small (metacarpal) bones of the centre of the hand.[neuro-chirurgie.org] […] difficulties Atrophy of intrinsic muscles of the hand Claw hand ("Hand of Benediction") Symptoms manifestation caused by entrapment and impingement of the ulnar nerve at[symptoma.com]

  • Scapuloperoneal Spinal Muscular Atrophy

    […] of face muscles Abnormality of limbs Clinodactyly Metatarsus adductus Peroneal muscle atrophy Peroneal muscle weakness Scapular muscle atrophy Small hand Talipes equinovarus[familydiagnosis.com] Symptoms of Scapuloperoneal spinal muscular atrophy Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Spasmodic torticollis Weakness[familydiagnosis.com]

  • Distal Hereditary Motor Neuropathy Type 2C

    small muscles of the hands. [3] Signs and symptoms [ edit ] Onset usually occurs within the first two decades of life, commonly in the teenage years or the twenties.[en.wikipedia.org] It is allelic (i.e., caused by mutations on the same gene) with Charcot–Marie–Tooth disease and with Silver’s Syndrome, a disorder also characterized by small muscle atrophy[en.wikipedia.org] Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance , weakness of the upper limbs that is progressive and symmetrical, and atrophy of the[en.wikipedia.org]

  • Distal Hereditary Motor Neuropathy Type 7A

    small muscles of the hands. [3] Signs and symptoms [ edit ] Onset usually occurs within the first two decades of life, commonly in the teenage years or the twenties.[en.wikipedia.org] It is allelic (i.e., caused by mutations on the same gene) with Charcot–Marie–Tooth disease and with Silver’s Syndrome, a disorder also characterized by small muscle atrophy[en.wikipedia.org] Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance , weakness of the upper limbs that is progressive and symmetrical, and atrophy of the[en.wikipedia.org]

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