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160 Possible Causes for Scapular Muscle Atrophy

  • 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] SP syndromes can resemble facioscapulohumeral muscular dystrophy (FSH) due to scapular weakness or Charcot-Marie-Tooth disease (CMT) due to atrophy of peroneal muscles.[ncbi.nlm.nih.gov] […] absence of muscles Progressive atrophy of scapular muscles and peroneal muscles (fibularis longus, brevis, and tertius) Progressive laryngeal muscle palsy Spinal muscular[amboss.com]

  • Hip Dysplasia Type Beukes

    […] weakness Skeletal muscle atrophy Torticollis Hyporeflexia Facial palsy Scapular winging Hoarse voice Limitation of joint mobility Lower limb muscle weakness Restrictive deficit[mendelian.co] muscle atrophy Need help with a diagnosis?[mendelian.co] […] fiber atrophy Gowers sign Nocturnal hypoventilation Increased muscle lipid content Laryngomalacia Dysphonia Limited neck flexion Weakness of facial musculature Axial muscle[mendelian.co]

  • West Nile Virus

    Clinical examination revealed marked periscapular, shoulder girdle, and humeral muscle atrophy and bilateral scapular winging, with near symmetrical bilateral hypotonic upper[ncbi.nlm.nih.gov]

  • Klippel-Trenaunay-Weber Syndrome

    […] right lower limb; and muscle atrophy on left lower limb with marked body asymmetry, scoliosis and toe malformations.[ncbi.nlm.nih.gov] We report a KTWS patient with extensive hemangiomatosis of the right lower limb, trunk and upper limbs; bone and soft tissue hypertrophy of upper limbs, scapular girdle and[ncbi.nlm.nih.gov]

  • Muscle-Eye-Brain Disease Type A14

    atrophy Eosinophilia Proximal amyotrophy Wrist flexion contracture Hamstring contractures Scapular muscle atrophy Reduced muscle fiber alpha dystroglycan Pelvic girdle amyotrophy[mendelian.co] Muscular hypotonia Obesity Joint stiffness Dyspnea Hypertrophic cardiomyopathy Ichthyosis Sudden cardiac death Hypertriglyceridemia Syncope Lumbar hyperlordosis Reduced muscle[mendelian.co] […] fiber merosin Fasciculations Congenital finger flexion contractures Steppage gait Autophagic vacuoles Juvenile onset Thoracic scoliosis Limited shoulder movement Limb-girdle muscle[mendelian.co]

  • Unilateral Hypoplasia or Absence of Pectoralis Major Muscle

    muscle atrophy Need help with a diagnosis?[mendelian.co] Hypoglycemia Feeding difficulties in infancy Acidosis Myoclonus Pneumonia Babinski sign Encephalopathy Patent ductus arteriosus Congestive heart failure Vomiting Fatigue Dystonia Scapular[mendelian.co]

  • Inclusion Body Myositis

    A 69-year-old man, who was a human T lymphotropic virus type 1 carrier, exhibited slowly progressive muscle weakness and atrophy, predominantly affecting the scapular, quadriceps[ncbi.nlm.nih.gov] There was inconspicuous scoliosis and atrophy of the scapular muscles.[scielo.br] […] femoris, and forearm flexor muscles.[ncbi.nlm.nih.gov]

  • Distal Spinal Muscular Atrophy Type 3

    […] absence of muscles Progressive atrophy of scapular muscles and peroneal muscles (fibularis longus, brevis, and tertius) Progressive laryngeal muscle palsy Spinal muscular[amboss.com] atrophy with respiratory distress type 1 Prevalence : 1 in 1,000,000 Etiology Defect in the IGHMBP2 ( immunoglobulin mu-binding protein 2) gene on chromosome 11q Autosomal[amboss.com] Scapuloperoneal spinal muscular atrophy Prevalence : 1 in 1,000,000 Etiology Defect in the TRPV4 gene on chromosome 12q Autosomal dominant inheritance Clinical features Congenital[amboss.com]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    […] absence of muscles Progressive atrophy of scapular muscles and peroneal muscles (fibularis longus, brevis, and tertius) Progressive laryngeal muscle palsy Spinal muscular[amboss.com] atrophy with respiratory distress type 1 Prevalence : 1 in 1,000,000 Etiology Defect in the IGHMBP2 ( immunoglobulin mu-binding protein 2) gene on chromosome 11q Autosomal[amboss.com] Scapuloperoneal spinal muscular atrophy Prevalence : 1 in 1,000,000 Etiology Defect in the TRPV4 gene on chromosome 12q Autosomal dominant inheritance Clinical features Congenital[amboss.com]

  • Adult Spinal Muscular Atrophy

    […] absence of muscles Progressive atrophy of scapular muscles and peroneal muscles (fibularis longus, brevis, and tertius) Progressive laryngeal muscle palsy Spinal muscular[amboss.com] atrophy with respiratory distress type 1 Prevalence : 1 in 1,000,000 Etiology Defect in the IGHMBP2 ( immunoglobulin mu-binding protein 2) gene on chromosome 11q Autosomal[amboss.com] Scapuloperoneal spinal muscular atrophy Prevalence : 1 in 1,000,000 Etiology Defect in the TRPV4 gene on chromosome 12q Autosomal dominant inheritance Clinical features Congenital[amboss.com]

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