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147 Possible Causes for EMG Shows Myopathic Pattern, Hyperbiliverdinemia

  • 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]

  • Hereditary North American Indian Childhood Cirrhosis

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

    Missing: EMG Shows Myopathic Pattern
  • Glycogen Storage Disease Type 9

    METHODS: Patient 1 (39 years old) had mild exercise-induced forearm pain, and EMG showed a myopathic pattern.[ncbi.nlm.nih.gov] Methods: Patient 1 (39 years old) had mild exercise-induced forearm pain, and EMG showed a myopathic pattern.[neurology.org]

    Missing: Hyperbiliverdinemia
  • Distal Myopathy Type 3

    The EMG shows a myopathic pattern and the muscle biopsy reveals dystrophic changes without the presence of rimmed vacuoles and absent dysferlin.[ruralneuropractice.com] The EMG showed a myopathic pattern.[scielo.br] The electromyography (EMG) showed a myopathic pattern with muscle biopsy taken from the vastus lateralis revealing dystrophic changes and Immunostaining showed evidence of[ruralneuropractice.com]

    Missing: Hyperbiliverdinemia
  • Limb-Girdle Muscular Dystrophy Type 1E

    EMG performed in right upper and lower limb showed myopathic pattern.[jcdr.net] Electromyography (EMG) showed myopathic pattern. He had elevated creatinine phosphokinase levels and muscle biopsy findings consistent with muscular dystrophy.[jcdr.net]

    Missing: Hyperbiliverdinemia
  • Transient Familial Neonatal Hyperbilirubinemia

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

    Missing: EMG Shows Myopathic Pattern
  • IgG4-Related Hepatopathy

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

    Missing: EMG Shows Myopathic Pattern
  • Congenital Enteropathy due to Enteropeptidase Deficiency

    […] syndrome Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary chronic pancreatitis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

    Missing: EMG Shows Myopathic Pattern
  • Familial Recurrent Peripheral Facial Palsy

    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]

    Missing: EMG Shows Myopathic Pattern
  • Overlap Syndrome

    Nerve conduction was normal, EMG showed typical myopathic pattern but the muscle biopsy showed a normal histology.[jpgmonline.com] In view of proximal and symmetrical muscle weakness, raised serum CPK, typical myopathic EMG and skin rash, this patient was diagnosed to have Polymyositis-Dematomyositis[jpgmonline.com]

    Missing: Hyperbiliverdinemia

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