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11 Possible Causes for Hyperbiliverdinemia, Myoclonic Jerking

  • Neuronal Ceroid Lipofuscinosis

    jerk and visual impairment.[ncbi.nlm.nih.gov] […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] Myoclonic jerks constituted the most prominent paroxysmal phenomenon.[ncbi.nlm.nih.gov]

  • 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] Arching of the head (exaggerated head-retraction reflex), jerking movements (myoclonic jerks) or falling stiffly to the ground without losing consciousness tends to occur[geneticdisordersuk.org] Hypertonia and generalized myoclonic jerks after stimulation, noted at 4 days of life, were associated with hypocalcemia.[pediatricneurologybriefs.com]

  • Hypertrichotic Osteochondrodysplasia

    jerks.[genomeweb.com] Cases 401948 Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency 4 Cases 168588 Hyperandrogenism due to cortisone reductase deficiency 11 Cases 276405 Hyperbiliverdinemia[azkurs.org] The trial was halted upon request subsequent to initiation of the first agent, diazepam, after complete resolution of nighttime myoclonic jerks.[docksci.com]

  • Gardner-Diamond Syndrome

    jerks, and dystonic muscle contractions.[physio-pedia.com] jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] dysfunction Studies have shown that approximately 70% of the patients with CRPS show muscle weakness in the affected limb, exaggerated tendon reflexes or tremor, irregular myoclonic[physio-pedia.com]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Epilepsy can develop into a serious and often fatal encephalopathy: myoclonic jerks or focal clonic seizures that progress to epilepsia partialis continua followed by status[ncbi.nlm.nih.gov] Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org]

  • Craniodiaphyseal Dysplasia

    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] […] dystonia Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks.[amp.pharm.mssm.edu] 15 Hypokalemic periodic paralysis, type 2 Migraine, familial basilar Howel-Evans syndrome Breast-ovarian cancer, familial 2 X-linked myopathy with postural muscle atrophy Myoclonic[amp.pharm.mssm.edu]

  • Schneckenbecken Dysplasia

    […] dystonia Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks.[amp.pharm.mssm.edu] 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] 15 Hypokalemic periodic paralysis, type 2 Migraine, familial basilar Howel-Evans syndrome Breast-ovarian cancer, familial 2 X-linked myopathy with postural muscle atrophy Myoclonic[amp.pharm.mssm.edu]

  • Glutamate Formiminotransferase Deficiency

    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] […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] […] dystonia Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks.[amp.pharm.mssm.edu]

  • Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome

    Raymond et al (2008) noted that M-D due to SGCE mutations is characterized by early onset myoclonic jerks, often associated with dystonia.[aetna.com] Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary fructose intolerance Hereditary hemorrhagic telangiectasia Hyperbiliverdinemia[se-atlas.de]

  • HSD10 Mitochondrial Disease

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] At 6 to 7 years of age, seizures also included brief myoclonic jerks.[journals.plos.org]

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