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98 Possible Causes for Increased Serum Creatine Phosphate, Phagocytic Vacuoles with Degraded Membranous Material

  • Myofibrillar Myopathy Type 3
  • Duchenne Muscular Dystrophy

    English Duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle Muscular dystrophy, Duchenne MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD Severe[…][wikidata.org]

    Missing: Phagocytic Vacuoles with Degraded Membranous Material
  • 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[…][oadoi.org]

    Missing: Phagocytic Vacuoles with Degraded Membranous Material
  • Becker Muscular Dystrophy

    The dystrophinopathies, which include Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and X-linked dilated cardiomyopathy, are X-linked recessive neuromuscular disorders caused by mutations in the dystrophin gene (DMD). Approximately 70% of mutations causing DMD/BMD are deletions or[…][ncbi.nlm.nih.gov]

    Missing: Phagocytic Vacuoles with Degraded Membranous Material
  • 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: Phagocytic Vacuoles with Degraded Membranous Material
  • 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: Phagocytic Vacuoles with Degraded Membranous Material
  • 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: Phagocytic Vacuoles with Degraded Membranous Material
  • Limb-Girdle Muscular Dystrophy Type 2E

    READ ORPHA.NET WEBSITE ABOUT BETA-SARCOGLYOCANOPATHY LIMB-GIRDLE MUSCULAR DYSTROPHIES (LGMD) Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetically determined disorders with a primary or predominant involvement of the pelvic or shoulder girdle musculature. The clinical course is[…][beta-sarcoglicanopathy.org]

    Missing: Phagocytic Vacuoles with Degraded Membranous Material
  • Limb-Girdle Muscular Dystrophy Type 1H

    Abstract Limb-girdle muscular dystrophies (LGMDs) are a genetically heterogeneous group of neuromuscular disorders with a selective or predominant involvement of shoulder and pelvic girdles. We clinically examined 19 members in a four-generation Italian family with autosomal-dominant LGMD. A total of 11 subjects were[…][doi.org]

    Missing: Phagocytic Vacuoles with Degraded Membranous Material
  • 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: Phagocytic Vacuoles with Degraded Membranous Material

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