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74 Possible Causes for Hyperbiliverdinemia, Seizure

  • Neuronal Ceroid Lipofuscinosis

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] Seizure severity did not vary by sex or genotype. Seizures showed mild worsening with increasing age.[ncbi.nlm.nih.gov] The symptoms appeared in two young adult siblings, and included progressive retinopathy, recurrent generalized seizures, moderate ataxia, and subtle cognitive dysfunction.[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] There are chapters on epileptic seizures that do not look like typical epileptic seizures, and conversely, apparent epileptic seizures that are not.[books.google.de] Due to its seizure-like presentation, it is usually misdiagnosed.[neurologyindia.com]

  • Autosomal Recessive Primary Microcephaly Type 10

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] PCH3 ( OMIM ) is characterized by hypotonia, hyperreflexia, microcephaly, optic atrophy, and seizures.[mendelian.co] Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.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] Among the medical signs are dacryocystitis, seizures, mental retardation, and paralysis, each of which is a complication resulting from the diminutive foramina.[wikidoc.org] […] a result of progressive bony overgrowth, intracranial pressure may increase and lead to brain and nerve compression, cranial nerve palsies, and an increased incidence of seizures[ncbi.nlm.nih.gov]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Aspects and Treatment of the HypoxicIschemic Syndrome 1160 137 Neuroprotective Strategies 1173 138 Cerebral Hemorrhage 1180 139 Neonatal Arterial Stroke 1192 140 Neonatal Seizures[books.google.com] Affected individuals tend to have respiratory insufficiency and seizures, and die in infancy.[mendelian.co]

  • 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] One such syndrome, involving generalized seizures in very young infants, is known as benign familial neonatal seizures.[epilepsy.com] If the condition is not treated, it can cause seizures and other severe brain problems.[diseaseinfosearch.org]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] Seizures of varying types, often including infantile spasms, are reported in most patients.[atlasgeneticsoncology.org] […] thrombocytopenia R enal: proteinuria, casts, hematuria, azotemia A NA I mmune abnormalities: LE cells, anti-dsDNA, anti-Smith, VDRL/RPR , decreased C3 N eurological Disease: seizures[pathologyexpert.com]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.org] Skin disease H00783 Febrile seizures Febrile seizures (FS), or febrile convulsions (FEB), are acute symptomatic seizures that occur in response to fever and represent the[kegg.jp] , Benign Familial Infantile, 4; BFIS4 OMIM:617080 Seizures, Benign Familial Infantile, 5; BFIS5 OMIM:121200 Seizures, Benign Familial Neonatal, 1; BFNS1 OMIM:121201 Seizures[informatics.jax.org]

  • 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] Seizure. 2009;18:104–8. PubMed CrossRef Google Scholar Nelles M, Bien CG, Kurthen M, von Falkenhausen M, Urbach H.[link.springer.com] Spastic dementia and seizures may eventually arise. Weakened bones (osteoporosis) are common and can result in fractures.[rarediseases.org]

  • Beta-Ureidopropionase Deficiency

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] Less than 10 patients have been reported, and the phenotype can range from severe neurologic involvement with mental retardation and seizures to normal neurologic development[diseaseinfosearch.org] People with beta-ureidopropionase deficiency can have low muscle tone (hypotonia), seizures, speech difficulties, developmental delay, intellectual disability, and autistic[ghr.nlm.nih.gov]

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