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170 Possible Causes for Hyperbiliverdinemia, Increased Serum Creatine Phosphate

  • Limb-Girdle Muscular Dystrophy Type 1H

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • 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: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia
  • Becker Muscular Dystrophy

    The rapid progress of research on the structure of the dystrophin gene has enormously increased our understanding of the molecular basis of Duchenne (DMD) and Becker (BMD) muscular dystrophy. Apart from "classical" clinical presentations, asymptomatic or only mildly affected individuals with deletions in the[…][ncbi.nlm.nih.gov]

    Missing: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia
  • 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: Hyperbiliverdinemia

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