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71 Possible Causes for Muscular Atrophy, Thenar Muscle Atrophy

  • Carpal Tunnel Syndrome

    Motor complaints relate to thenar muscular weakness and atrophy.[] At the six-month follow-up examination, the patient experienced relief from numbness and improvement in thenar muscle atrophy was noted.[] (particularly peroneal muscular atrophy) resulting in foot dorsiflexor weakness, foot drop, and secondary steppage gait.[]

  • Cervical Spondylosis

    […] groups, especially in the extremities poor or pathologic tandem gait atrophy of the hand’s thenar prominence (the fleshy fat pad just superior to the thumb on the ventral[] […] the following: clonus or spasticity of the lower extremities sensory changes (light touch, pinprick sensation, or temperature dysfunction) generalized weakness throughout muscle[]

  • Iatrogenic Cushing's Disease

    Prevalence rate of the other clinical features such as polyphagia, abdominal enlargement, panting, muscular atrophy, prominent vasculature, calcinosis cutis and thin skin[] atrophy Spinal stenosis Spinocerebellar ataxia Spleen Splenic rupture Splenomegaly Spondylolisthesis Sports injuries Staphylococcal diseases Staphylococcal scalded skin syndrome[] Sodium disorders Soft tissue lesions of the shoulder Somatic symptom and related disorders Spasticity Specialized nutrition support Spinal cord tracts and reflexes Spinal muscular[]

  • Distal Hereditary Motor Neuropathy Type 5

    Spinal muscular atrophy: a clinical and research update. Pediatr Neurol. 2012;46(1):1-12. 5. Muscular Dystrophy Association. Spinal muscular atrophy. Types of SMA. .[] Treatment for spinal muscular atrophy Unfortunately, there is currently no specific treatment for SMA.[] Marked facial weakness is observed in these patients with congenital myopathies. [2] Spinal Muscular Atrophy Distal spinal muscular atrophy is an autosomal recessive infantile[]

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] […] and weakness of the thenar muscle group.[] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[]

  • Polyneuropathy

    Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy. Hum. Mol.[] […] and weakness of the thenar muscle group.[] Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography .[]

  • Median Neuropathy

    atrophy (axonal type) (hypertrophic type) Roussy-Levy syndrome diabetic - see E08-E13 with .40 mononeuropathy - see E08-E13 with .41 polyneuropathy - see E08-E13 with .42[] muscle atrophy may occur.[] 354.0 ICD10 G56.0, G56.00 SnomedCT 155073007, 193126005, 57406009, 246611002 English Carpal Tunnel Syndromes, Syndromes, Carpal Tunnel, Syndrome, Carpal Tunnel, AMYOTROPHY, THENAR[]

  • Distal Myopathy Type 3

    Marked facial weakness is observed in these patients with congenital myopathies. [2] Spinal Muscular Atrophy Distal spinal muscular atrophy is an autosomal recessive infantile[] Spinal muscular atrophies: Amyotrophic lateral sclerosis (ALS), or motor neuron disease Infantile progressive spinal muscular atrophy Intermediate spinal muscular atrophy[] atrophy ( 1 Files ) Disease name: Spinal muscular atrophy ICD 10 : G12.0 Infantile spinal muscle atrophy type I G12.1 Spinal muscle atrophy childhood form type II G12.1 Spinal[]

  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[] […] group of muscles, including the abductor pollicis brevis (APB) and first dorsal interosseous (FDI), when compared to the abductor digit minimi (ADM) [Figure 1]. 14,22 This[] KEYWORDS: Lower motor neuron syndrome; Lower motor neuron-onset ALS; PMA; Progressive muscular atrophy[]

  • Autosomal Dominant Spastic Paraplegia Type 17

    SPG17 is a motor neuron disease overlapping with distal spinal muscular atrophy type 5.[] Disease description A disorder characterized by distal muscular atrophy mainly affecting the upper extremities, in contrast to other distal motor neuronopathies.[] The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss.[]

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