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120 Possible Causes for Increased Serum Creatine Phosphate, Myoglobinuria after Exertion

  • 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]

  • 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] It usually presents with episodic cramps, weakness or myoglobinuria after exertion or prolonged exercise.[annalsofneurosciences.org] […] should be treated aggressively by increasing the fluid intake.[clinicalgate.com]

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    It usually presents with episodic cramps, weakness or myoglobinuria after exertion or prolonged exercise.[annalsofneurosciences.org] […] muscle fatigue, myalgia, muscle cramps, muscle swelling; myoglobinuria due to rhabdomyolysis may occur after exercise; severe myoglobinuria may lead to acute renal failure[clinicaladvisor.com] […] hypoglycemia; hypotonia, muscle atrophy; amylopectin-like inclusions; respiratory insufficiency; may have cardiomyopathy or neuronal involvement Type V Muscle glycogen phophorylase Exertional[clinicaladvisor.com]

  • Glycogen Storage Disease Type 3

    […] muscle fatigue, myalgia, muscle cramps, muscle swelling; myoglobinuria due to rhabdomyolysis may occur after exercise; severe myoglobinuria may lead to acute renal failure[clinicaladvisor.com] […] hypoglycemia; hypotonia, muscle atrophy; amylopectin-like inclusions; respiratory insufficiency; may have cardiomyopathy or neuronal involvement Type V Muscle glycogen phophorylase Exertional[clinicaladvisor.com]

  • 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: Myoglobinuria after Exertion
  • 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: Myoglobinuria after Exertion
  • 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: Myoglobinuria after Exertion
  • 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: Myoglobinuria after Exertion
  • Limb-Girdle Muscular Dystrophy Type 1E

    Limb-girdle muscular dystrophies (LGMD) are heterogeneous disorders with autosomal inheritance. Autosomal dominant LGMD mapped to 7q36.3 has been classified as LGMD type 1D (LGMD1D) in the Human Gene Nomenclature Committee Database. LGMD1D is characterized predominantly by limb-girdle weakness and may also show a[…][ncbi.nlm.nih.gov]

    Missing: Myoglobinuria after Exertion
  • 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: Myoglobinuria after Exertion

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