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4,156 Possible Causes for No Muscle Weakness, Pediatric Disorder

  • Vitamin D Deficiency

    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] 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] All had generalized bone pain and tenderness, muscle weakness, stooping posture, difficulty walking, and waddling gait due to severe proximal muscle weakness for a period[ncbi.nlm.nih.gov]

  • 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] Occasionally, however, females who carry a DMD gene mutation may have muscle weakness and cramping.[ghr.nlm.nih.gov] Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Acsadi G. Duchenne Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.org]

  • 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] Breath stacking in children with neuromuscular disorders. Pediatr Pulmonol . 2013 Aug 16. [Medline] .[emedicine.medscape.com]

  • Facioscapulohumeral Muscular Dystrophy

    Complications of Neuromuscular Disorders. In Epp, Jr., CH & Bowen Jr., Complications in Pediatric Orthopaedic Surgery, 627-630,1995 Tachdjian M.O.[gait.aidi.udel.edu] BACKGROUND: Although muscle weakness is a hallmark of facioscapulohumeral muscular dystrophy (FSHD), the molecular mechanisms that lead to weakness in FSHD remain largely[ncbi.nlm.nih.gov] Neuromuscul Disord. 2016 Jul;26(7):405-13. doi: 10.1016/j.nmd.2016.04.012. Epub 2016 Apr 22.[ncbi.nlm.nih.gov]

  • 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] Muscle weakness may spread from the proximal muscles to affect distal muscles.[rarediseases.org]

  • Glycogen Storage Disease Type 2

    Dyspnea secondary to diaphragm or respiratory muscle weakness may also be observed.[symptoma.com] Nomenclature for Conditions based upon “Naming and Counting Disorders (Conditions) Included in Newborn Screening Panels.” Pediatrics. 2006; 117 (5) Suppl: S308-S314.[hrsa.gov] Dowling, Myopathies and Myotonic Disorders, Pediatric Electromyography, 10.1007/978-3-319-61361-1_22, (327-354), (2017). G. Chalès and P.[dx.doi.org]

  • Paramyotonia Congenita

    Kang, The Spectrum of Myotonic and Myopathic Disorders in a Pediatric Electromyography Laboratory Over 12 Years, Pediatric Neurology, 47, 2, (97), (2012).[doi.org] The resulting increase in ion flow interferes with normal muscle contraction and relaxation, leading to episodes of muscle stiffness and weakness.[ghr.nlm.nih.gov] - Current Pediatric Research (2010) Volume 14, Issue 1 Paramyotonia Congenita is a rare neuromuscular disorder characterized by paradoxical myotonia.[alliedacademies.org]

  • Myotonic Dystrophy

    On neurological examination the patient was presented with muscle weakness, muscle atrophy (in face and sternocleidomastoid muscles), features of myotonia and apocamnosis[ncbi.nlm.nih.gov] Pediatr Neurol. 1994; 11:208. [ Links ] 9. D’Angelo MG, Bresolin N. Cognitive impairment in neuromuscular disorders. Muscle Nerve. 2006; 34:16. 10.[scielo.mec.pt] Often, the disorder is mild and only minor muscle weakness or cataracts are seen late in life.[web.archive.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] Definition: Juvenile dermatomyositis or JDM is an autoimmune disorder which causes vasculitis manifesting itself among children; and it is a pediatric equivalent of dermatomyositis[web.archive.org]

  • Spinal Muscular Atrophy

    The Pediatric SMA Clinical Research Center, which operates conjointly with the Pediatric Neuromuscular Clinic at Columbia University, is organized according to a team model[columbiasma.org] We report the case of a male who presented in infancy with motor delay and muscle weakness.[ncbi.nlm.nih.gov] Our pediatric endocrinologists provide family-centered care for children and adolescents with type 1 and type 2 diabetes, adrenal and thyroid disorders, gender disorders,[dukechildrens.org]

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