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235 Possible Causes for Gowers Sign, No Muscle Weakness, Pediatric Disorder

  • Duchenne Muscular Dystrophy

    BACKGROUND AND PURPOSE: Duchenne muscular dystrophy (DMD) is a lethal progressive pediatric muscle disorder and genetically inherited as an X-linked disease that caused by[ncbi.nlm.nih.gov] Muscle weakness Other names Myasthenia Specialty Neurology Muscle weakness is a lack of muscle strength.[en.wikipedia.org] She exhibited Gowers' sign, calf muscle hypertrophy, and a high serum creatine kinase level at 2 years.[ncbi.nlm.nih.gov]

  • Becker Muscular Dystrophy

    Little is known about parental motivations and expectations for clinical trials for rare pediatric disorders.[ncbi.nlm.nih.gov] Later symptoms Muscle weakness: Affects the proximal muscles of the limbs mainly.[patient.info] From age 27 years, he developed proximal muscle weakness predominantly of the lower limbs, a positive Gower sign, and a waddling gait.[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease Type 2

    Nomenclature for Conditions based upon “Naming and Counting Disorders (Conditions) Included in Newborn Screening Panels.” Pediatrics. 2006; 117 (5) Suppl: S308-S314.[hrsa.gov] Dyspnea secondary to diaphragm or respiratory muscle weakness may also be observed.[symptoma.com] The patient presented unmistakable signs of muscular atrophy in the upper and lower limbs, as well as positive Gowers' sign. Levels of creatinkinase in serum were high.[ncbi.nlm.nih.gov]

  • Vitamin D Deficiency

    Hypocalcemic and hypercalcemic disorders in children . Current Problems in Pediatrics, Vol. 19, Issue. 10, p. 497. CrossRef Google Scholar Poskitt, E.M.E. 1988.[doi.org] Apart from the well-known effects on bone metabolism, this condition is also associated with muscle weakness, predominantly of the proximal muscle groups.[ncbi.nlm.nih.gov] ’s sign can provide an early clue (representing proximal myopathy).[rcpch.ac.uk]

  • Erb Muscular Dystrophy

    Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics. 7th ed.[emedicine.medscape.com] Weakness is generally asymmetric and may spare the deltoid, supraspinatus, and infraspinatus muscles.[checkorphan.org] Contractures Tachypnea and shortness of breath Assessment-Duchenne and Becker's types Wide stance and waddling gait Gowers' sign when rising from a sitting or supine position[quizlet.com]

  • Muscular Dystrophy

    We offer children and families coordinated care for the diagnosis and treatment of muscular dystrophy and other pediatric neuromuscular disorders.[ynhh.org] It causes progressive weakness in muscles of the face, arms, legs, and around the shoulders and chest.[ninds.nih.gov] ’s sign of proximal muscle weakness 1.[radiopaedia.org]

  • Childhood Dermatomyositis

    […] doi: 10.1097/01.bor.0000240362.32089.4c Pediatric and heritable disorders Abstract Author Information Authors Article Metrics Metrics Juvenile dermatomyositis is a rare chronic[journals.lww.com] In a second flare in childhood, she developed proximal muscle weakness and calcinosis cutis. A muscle biopsy was consistent with juvenile dermatomyositis.[ncbi.nlm.nih.gov] Many children exhibit the Gower sign, with difficulty rising from the floor due to hip extensor weakness, using the hands to climb up the legs as an aid.[obgynkey.com]

  • Muscular Dystrophy-Dystroglycanopathy Type C4

    Greatly expanded sections to increase your knowledge of perinatal acquired and congenital disorders, neurodevelopmental disabilities, pediatric epilepsy, and nonepileptiform[books.google.de] In addition to proximal muscle weakness, there may or may not be: Distal muscle weakness. Muscle hypertrophy. Contractures.[patient.info] sign 0003391 Increased variability in muscle fiber diameter 0003557 Myopathic facies 0002058 Myopathy Muscle tissue disease 0003198 Pelvic girdle muscle weakness 0003749[rarediseases.info.nih.gov]

  • Limb-Girdle Muscular Dystrophy Type 2C

    Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Ascadi G. Limb-Girdle Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.org] Limb-girdle muscular dystrophy includes a group of inherited disorders that cause muscle weakness and decreased amount of skeletal muscle involving the muscles around the[geneaware.clinical.bcm.edu] Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported.[orpha.net]

  • Muscular Dystrophy-Dystroglycanopathy Type C3

    Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Ascadi G. Limb-Girdle Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.org] Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported.[orpha.net] Image : “Gower’s sign.” by William Richard Gowers (1845–1915) – Gowers WR. Clinical lecture on pseudohypertrophic muscular paralysis. Lancet 1879;ii,73-5.[lecturio.com]

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