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107 Possible Causes for Increased Serum Creatine Phosphate, Subsarcolemmal Accumulation of Normal Mitochondria

  • Danon Disease

    There was an increase in glycogen granules with subsarcolemmal accumulation.[circ.ahajournals.org] Mitochondria appeared to be of normal density with no demonstrable abnormal cristae pattern or intramitochondrial inclusions.[circ.ahajournals.org]

  • Duchenne Muscular Dystrophy

    The longer survival of patients with Duchenne muscular dystrophy due to advances in clinical care has increased the incidence of Duchenne muscular dystrophy-associated cardiomyopathy, a nearly consistent feature in the third decade of life. A 26-year-old patient with Duchenne muscular dystrophy experienced[…][ncbi.nlm.nih.gov]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Spinal and Bulbar Muscular Atrophy

    Abstract Introduction: Spinobulbar muscular atrophy (SBMA) is an inherited adult‐onset motor neuron disease caused by the expansion of a polyglutamine tract within the androgen receptor. Autonomic nervous system involvement (ANS) is not considered part of SBMA. The aim of this study was to assess autonomic[…][dx.doi.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Becker Muscular Dystrophy

    Becker and Kiener initially described Becker muscular dystrophy (BMD) in 1955. [1, 2] BMD is an inherited disease with a male distribution pattern and a clinical picture similar to that of Duchenne muscular dystrophy (DMD). BMD is generally milder than DMD, and the onset of symptoms usually occurs later. The clinical[…][emedicine.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Careful monitoring of the serum creatine kinase and phosphate levels is essential. Intravenous fluids, furosemide, and hemodialysis are sometimes required.[clinicalgate.com] […] should be treated aggressively by increasing the fluid intake.[clinicalgate.com] There is evidence that an oral sucrose load before activity can increase exercise tolerance, but this may not be practical in every circumstance. 12 Myoglobinuria and rhabdomyolysis[clinicalgate.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Muscular Dystrophy-Dystroglycanopathy Type C14

    1 A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies. ( 23687351 ) 2013 2 Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy. ( 21109228 )[…][malacards.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Muscular Dystrophy-Dystroglycanopathy Type C2

    Primary Outcome Measures : MRI scan for qualitative analysis of muscle involvement [ Time Frame: One MRI scan per subject (exam lasts approximately 60 min.) ] The MRI protocol include T1-weighted brain and whole body examination. Four cross-sectional slices at shoulder, lumbar back, thigh and calf are chosen for[…][clinicaltrials.gov]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Emery-Dreifuss Muscular Dystrophy Type 1

    Neuropediatrics 2017; 48(S 01): S1-S45 DOI: 10.1055/s-0037-1603007 Georg Thieme Verlag KG Stuttgart · New York O. Schwartz 1 Universitätsklinikum Münster, Klinik für Kinder- und Jugendmedizin, Allgemeine Pädiatrie, Bereich Neuropädiatrie, Deutschland J. Althaus 1 Universitätsklinikum Münster, Klinik für Kinder- und[…][thieme-connect.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Muscular Dystrophy-Dystroglycanopathy Type C7

    Arthur G. Steinberg, Alexander G. Bearn Butterworth-Heinemann, 11.09.2013 - 160 Seiten Progress in Medical Genetics: Volume 5 covers the improvements in nutrition and control of childhood disease. This book is divided into five chapters that evaluate the characteristics of thalassemias, an inherited defect in[…][books.google.de]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Limb-Girdle Muscular Dystrophy Type 1G

    Vikram Patel, Alistair Woodward, Valery Feigin, Stella R. Quah, Kristian Heggenhougen Academic Press, ٠٧‏/٠٦‏/٢٠١٠ - 560 من الصفحات Colin Mathers who leads the Global Burden of Disease group in WHO has confirmed that, in the 2004 GBD, 13.1% of global Daily Adjusted Life Years are attributable to mental or neurological[…][books.google.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria

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