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1,056 Possible Causes for Alpers Syndrome

  • Alpers Syndrome

    Entry H01389 Disease Name Alpers syndrome; Alpers-Huttenlocher syndrome; Diffuse cerebral sclerosis of Schilder; Hepatocerebral degeneration of childhood; Mitochondrial DNA[] Alpers syndrome is a rare disease which occurs in about 1:100,000 to 1:250,000 individuals. Alpers syndrome occurs in both sexes.[] Cerebral Sclerosis of Schilder Eye Diseases Female Follow-Up Studies Genotype Glial Fibrillary Acidic Protein Humans Immunohistochemistry Infant Intellectual Disability Liver[]

  • Diffuse Cerebral Sclerosis of Schilder

    Concentric sclerosis of Balo is differentiated from diffuse cerebral sclerosis of Schilder by the pathologic finding of alternating bands of destruction and preservation of[] Diseases, CNS Diffuse Cerebral Sclerosis of Schilder[] Schilder" by people in Harvard Catalyst Profiles by year, and whether "Diffuse Cerebral Sclerosis of Schilder" was a major or minor topic of these publication.[]

  • Mitochondrial DNA Depletion Syndrome

    Additional phenotypes include fatal infantile lactic acidosis with methylmalonic aciduria, spastic ataxia (early-onset spastic ataxia-neuropathy syndrome), and Alpers syndrome[] Alpers syndrome is characterised by intractable epilepsy and liver dysfunction, but either problem can present in isolation.[] Alpers syndrome and related hepatocerebral disorders constitute the most common subgroup of MDDS, caused by mutations in the POLG gene encoding the catalytic subunit of the[]

  • Baló Concentric Sclerosis

    Concentric sclerosis of balo is differentiated from diffuse cerebral sclerosis of schilder by the pathologic finding of alternating bands of destruction and preservation of[] Concentric sclerosis of Balo is differentiated from diffuse cerebral sclerosis of Schilder by the pathologic finding of alternating bands of destruction and preservation of[] cerebral sclerosis of Schilder Concentric demyelination Marburg variant Tumefactive multiple sclerosis[]

  • Mitochondrial Neurogastrointestinal Encephalomyopathy

    Saneto RP, Cohen BH, Copeland WC and Naviaux RK (2013) Alpers‐Huttenlocher syndrome. Pediatric Neurology 48: 167–78.[] Entry H00469 Disease Name Mitochondrial DNA depletion syndrome Subgroup Alpers syndrome [DS: H01389 ] MNGIE syndrome [DS: H01390 ] Supergrp Mitochondrial disease [DS: H01427[] This form of MDDS is also called "Alpers' disease", also called "Alpers' syndrome", "Alpers-Huttenlocher syndrome", "progressive sclerosing poliodystrophy", and "progressive[]

  • Ovarian Cyst

    Alper MM, Smith LP, Sills ES (2009) Ovarian hyperstimulation syndrome: current views on pathophysiology, risk factors, prevention, and management.[] Keywords Dilatation and evacuation Human chorionic gonadotropin Molar pregnancy OHSS Ovary hyperstimulation syndrome This is a preview of subscription content, log in to check[]

  • Autosomal Dominant Progressive External Ophthalmoplegia Type 6

    Autosomal-recessive POLG mutations lead to a broader spectrum of clinical phenotypes ranging from Alpers syndrome to ataxia-neuropathy syndrome with or without epilepsy to[] […] type 4A (Alpers syndrome) and sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (SANDO).[] 390 OPA3 Optic atrophy, 3-methylglutaconic aciduria AD/AR 13 15 POLG POLG-related ataxia neuropathy spectrum disorders, Sensory ataxia, dysarthria, and ophthalmoparesis, Alpers[]

  • Obesity

    Alper Otunctemur, Murat Dursun, Emin Ozbek, Suleyman Sahin, Huseyin Besiroglu, Ismail Koklu, Mustafa Erkoc, Eyyup Danis and Muammer Bozkurt, Impact of metabolic syndrome on[]

  • Restless Legs Syndrome

    […] of restless legs syndrome (RLS) in the elderly and the relation of serum ferritin levels with disease severity: Hospital-based study from Istanbul, Turkey, Archives of Gerontology[] Aslı Çurgunlu, Alper Döventaş, Derya Karadeniz, Deniz Suna Erdinçler, Ayşe Kutlu Öztürk, Yesari Karter, Adnan Yaldıran, Fikret Sipahioğlu and Tanju Beğer, Prevalence and characteristics[]

  • Hereditary Myopathy with Lactic Acidosis due to ISCU Deficiency

    syndrome hepatocerebral form nuclear DNA synthesis (S phase) dnt2 adenosine DGUOK MPV17 hepatocerebral form NDP RNR dntp dndp mtdna TK2 muscular form de novo synthesis POLG[] NDUFS1 Mitochondrial complex I deficiency OPA1 Glaucoma, normal tension OPA3 3-methylglutaconic aciduria, Optic atrophy POLG Alpers syndrome, Mitochondrial DNA depletion[] syndrome, Progressive external ophthalmoplegia with mitochondrial DNA deletions, Mitochondrial DNA depletion syndrome AD/AR 89 290 POLG2 Progressive external ophthalmoplegia[]

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