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246 Possible Causes for Creatine Phosphokinase Increased, 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] 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] High serum creatine kinase Increased CPK Increased creatine kinase Increased creatine phosphokinase Increased serum CK Increased serum creatine kinase Increased serum creatine[rarediseases.info.nih.gov] Later symptoms Muscle weakness: Affects the proximal muscles of the limbs mainly.[patient.info]

  • 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] 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]

  • 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]

  • Glycogen Storage Disease Type 5

    Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[books.google.com] One hallmark of McArdle disease is weakness with exertion. Proximal muscle weakness may progress with time, and no specific treatment exists.[emedicine.com] As Tarnopolsky remarks, “There is rarely a definitive answer in rare disorders.”[mda.org]

  • Myotonia Congenita

    […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro] A 56-year-old woman was referred to a neurogenetic clinic with a history of stiffness and transient weakness.[ncbi.nlm.nih.gov] Deymeer F et al . (1998) Transient weakness and compound muscle action potential decrement in myotonia congenita . Muscle Nerve 21 : 1334–1337 7.[nature.com]

  • Glycogen Storage Disease Type 7

    Manley, Disorders of Erythrocyte Metabolism Including Porphyria, Pediatric Hematology, (171-212), (2007). J. N. Fleming‐Waddell, L. M. Wilson, G. R. Olbricht, T.[doi.org] Our observation suggests that juvenile-onset fixed muscle weakness may be a predominant clinical feature of PFK deficiency.[ncbi.nlm.nih.gov] , Germany 3 Laboratory of Metabolic Disorders and Molecular Genetics, Munich, Germany 4 Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Academic Medical[thieme-connect.com]

  • Kearns-Sayre Syndrome

    […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro] […] lactic acid, creatine phosphokinase and protein in CSF, abnormal electroretinography and visual-evoked potential testing.[jmedicalcasereports.biomedcentral.com] His manifestations included progressive external ophthalmoplegia, bilateral ptosis, retinitis pigmentosa, and muscle weakness.[ncbi.nlm.nih.gov]

  • Diabetic Ketotic Coma

    weakness.[endocrinologyadvisor.com] You’ll benefit from unique, global perspectives on adult and pediatric endocrinology prepared by an international team of renowned authorities.[books.google.com] Special considerations in hypoglycemic patients include alcohol abuse, the pediatric population, and conditions involving no IV access.[ahcmedia.com]

  • Juvenile Myxedema

    Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.de] weakness, delayed relaxation of tendon reflexes, and sometimes myxedema. [ hypo- G. thyreoeidēs, thyroid] hypothyroidism Underactivity of the THYROID GLAND.[medical-dictionary.thefreedictionary.com] Pediatr Ann 1992; 21: 29-35. 2. Foley TP Jr. Disorders of the thyroid in children. ln: (ed) Pediatrics Endocrinology, 1st edn. Philadelphia, W.B.[indianpediatrics.net]

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