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1,194 Possible Causes for No Muscle Weakness, Pediatric Disorder, Proximal Muscle Weakness

  • Vitamin D Deficiency

    We report a four-year-old African boy referred for proximal muscle weakness, fatigability and episodic limb pain.[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] 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]

  • Childhood Dermatomyositis

    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] […] 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] 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]

  • Facioscapulohumeral Muscular Dystrophy

    We report a 12-year-old patient with mental impairment and proximal muscle weakness who had marked involvement of the shoulder girdle and facial muscles.[ncbi.nlm.nih.gov] 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]

  • Glycogen Storage Disease Type 2

    Progressive proximal muscle weakness including major impairment of respiratory function dominates the picture.[ommbid.mhmedical.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] Dyspnea secondary to diaphragm or respiratory muscle weakness may also be observed.[symptoma.com]

  • Hypokalemic Periodic Paralysis

    She developed significant proximal muscle weakness within 16 hours after the initial dose. Her serum potassium was 1.6 mEq/L.[ncbi.nlm.nih.gov] The disorder has been described most frequently in Asian males.[pediatrics.aappublications.org] Two cases had a history of recurrent episodes of muscle weakness and difficulty in running before their first paralytic attack.[ncbi.nlm.nih.gov]

  • Bartter's Disease

    Clinical findings Proximal muscle weakness, failure to thrive, short stature, convulsions, tetany, cramps, ileus, gout, mental retardation, enuresis, nocturia, polyuria, salt[medical-dictionary.thefreedictionary.com] Disorders of renal transport of sodium, potassium and magnesium. In Pediatric Kidney Disease, Vol. 2, 1st edition. CM Edlemann Jr, editor.[jpgmonline.com] Tubular Disorders of Electrolyte Regulation. Pediatric Nephrology. Ellis D. Avner, William E. Harmon, Patrick Niaudet, Norishige Yoshikawa (Eds.).[revistas.unimilitar.edu.co]

  • Becker Muscular Dystrophy

    A Thai 37-years-old man presented with adult onset progressive proximal muscle weakness and generalized myalgia.[ncbi.nlm.nih.gov] 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]

  • Camurati-Engelmann Syndrome

    The proband is a 17-year-old woman who presented with lower limb pain and proximal muscle weakness.[semanticscholar.org] Pediatrics 1984 ; 74 : 399 –405. 3 Crisp AJ, Brenton DP. Engelmann's disease of bone—a systemic disorder?[academic.oup.com] Patients generally present with pain in the extremities, waddling gait, easy fatigability, and muscle weakness.[orpha.net]

  • Duchenne Muscular Dystrophy

    We report a 40-yr-old woman who presented with subacute proximal muscle weakness and high serum level of creatine kinase.[ncbi.nlm.nih.gov] 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]

  • X-Linked Hypophosphatemia

    Generalized muscle weakness is the most common symptom across all types of familial hypophosphatemia, while myalgia and fatigue are invariably present.[symptoma.com] Genetic disorders of phosphate regulation. Pediatr Nephrol. 2012;27(9):1477-87. Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL.[rarediseases.org] muscle weakness for 8 years.[casereports.bmj.com]

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