Create issue ticket

138 Possible Causes for Hyperbiliverdinemia, Subsarcolemmal Mitochondrial Accumulation

  • Limb-Girdle Muscular Dystrophy Type 1H

    Two muscle biopsies showed morphological findings compatible with MD associated with subsarcolemmal accumulation of mitochondria and the presence of multiple mitochondrial[moh-it.pure.elsevier.com] 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 Myopathy with Lactic Acidosis due to ISCU Deficiency

    Abstract Recently, we described a patient with severe exercise intolerance and episodic myoglobinuria, associated with marked impairment of succinate oxidation and deficient activity of succinate dehydrogenase and aconitase in muscle mitochondria (1). We now report additional enzymatic and immunological[…][jci.org]

    Missing: Hyperbiliverdinemia
  • 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: Subsarcolemmal Mitochondrial Accumulation
  • 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: Subsarcolemmal Mitochondrial Accumulation
  • 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: Subsarcolemmal Mitochondrial Accumulation
  • 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: Subsarcolemmal Mitochondrial Accumulation
  • 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: Subsarcolemmal Mitochondrial Accumulation
  • Granulomatous Mastitis

    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: Subsarcolemmal Mitochondrial Accumulation
  • Hereditary Hyperekplexia

    Joubert syndrome 17 Cardiac conduction defect, nonspecific Lethal multiple pterygium syndrome Non-small cell lung cancer Acroerythrokeratoderma Renal hypodysplasia/aplasia 2 Hyperbiliverdinemia[amp.pharm.mssm.edu]

    Missing: Subsarcolemmal Mitochondrial Accumulation
  • MELAS Syndrome

    mitochondrial accumulations Widespread EM abnormalities in any tissue Enzymology 30–40% activity of ay RC complex in a cell line 30–40% activity of the same RC complex in[academic.oup.com] In children with mitochondrial diseases, true RRF are a rare finding but subsarcolemmal accumulations of mitochondria are much more common, and often increase with the age[scielo.br] Molecular Identification of a nuclear or mtDNA mutation of undisputed pathogenicity Minor Clinical Symptoms compatible with a RC defect Histology Any ragged red fibres 2% subsarcolemmal[academic.oup.com]

    Missing: Hyperbiliverdinemia

Further symptoms

Similar symptoms