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61 Possible Causes for Lactic Acidosis, Prominent Sulci

  • Hypoxia

    Grossly, the lesion was marked by preserved gyral crests and involved sulci, resulting in prominent, mushroom-shaped gyri.[] The book then proceeds to a description of the situations in which hypoxic metabolic acidosis develops, such as during high altitude exposure, cardiac arrest, and lactic acidosis[] So basically, we're getting into a state of metabolic acidosis.[]

  • Combined Oxidative Phosphorylation Defect Type 11

    Types of lactic acidosis Cohen and Woods divided lactic acidosis into 2 categories, type A and type B. [5, 7] Type A is lactic acidosis occurring in association with clinical[] OMIM : 57 COXPD11 is a severe multisystemic autosomal recessive disorder characterized by neonatal hypotonia and lactic acidosis.[] Diseases related with Visual impairment and Lactic acidosis In the following list you will find some of the most common rare diseases related to Visual impairment and Lactic[]

  • Cerebral Cortical Atrophy

    Imaging wise feature of cerebral cortical atrophy Generalized prominence of hemisphere cortical sulci on CT or MRI in mild cases.[] Most cases present with neonatal-onset hypotonia, lactic acidosis, hyperammonemia, hypertrophic cardiomyopathy, and 3-methylglutaconic aciduria.[] Characteristic features include prominent cerebral sulci (i.e. cortical atrophy) and v entriculomegaly (i.e. central atrophy) without bulging of the third ventricular recesses[]

  • Congenital Cataract

    Brain imaging has revealed large ventricles, with subcortical hypomyelination, a thin corpus callosum, and prominent cortical sulci.[] The syndrome of hypertrophic cardiomyopathy, mitochondrial myopathy, congenital cataract, and lactic acidosis is a rare disease.[] acidosis.[]

  • Methylmalonic Acidemia

    CT on the same day of admission depicted mild prominence of the cortical sulci and ventricular system.[] After hemodialysis and clearance of toxic metabolites, severe lactic acidosis persisted with multiorgan failure.[] Biological investigations showed a hyperglycemia, a lactic acidosis and a hyperammonemia.[]

  • Beta-Ureidopropionase Deficiency

    MRI at 2 years showed dilated ventricles, prominent cortical sulci and incomplete myelination.[] […] hypertension syndrome Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Fatal infantile lactic acidosis with methylmalonic aciduria Fatal[] acidosis Acyl-CoA dehydrogenase 9 deficiency Hereditary myopathy with lactic acidosis due to ISCU deficiency Fatal infantile hypertrophic cardiomyopathy due to mitochondrial[]

  • Toluene Poisoning

    C, Sagittal T1-weighted (600/15/1) midline image shows thinning of the corpus callosum, which is more prominent in the body and genu. Note the enlarged cerebellar sulci.[] Keywords: Lactic acidosis, toluene, hyperlactemia How to cite this article: Omar AS, Rahman Mu, Abuhasna S.[] Clinicians should have a high index of suspicion in children with a metabolic acidosis particularly if ketoacidosis, lactic acidosis and renal failure have been excluded.[]

  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

    sulci and fissures, subcortical cystlike lesions shown on T1-weighted images, and hyperintense lesions at the periventricular white matter shown on T2-weighted images ( 5[] Sections deal with: (1) Lactic acidosis due to PDH deficiency and to complex I deficiency with MELAS; (2) Organic acidaemias including case reports, analytical approaches[] Hyper-uricemia Hyper lipidemia Adverse response to Glucagon with worsening Lactic acidosis.[]

  • Muscular Dystrophy-Dystroglycanopathy Type C2

    There was mild cerebellar volume loss with the prominence of median sulci, cerebellar folia, and ex vacuo dilatation of the fourth greater than bodies of the lateral ventricles[] acidosis syndrome Carnitine palmitoyl transferase 1A deficiency Carnitine palmitoyl transferase II deficiency, myopathic form Carnitine palmitoyl transferase II deficiency[] […] ophthalmoplegia, with mtDNA deletions, autosomal dominant 3 (C10ORF2, TWINKLE) MITOCHONDRIAL DISORDERS (MITOCHONDRIAL GENOME MUTATION CAUSED) Mitochondrial Encephalomyopathy, Lactic[]

  • Chronic Daily Headaches

    acidosis and stroke-like episodes), a rare genetic disorder caused by point mutations in the mitochondrial DNA that lead to a taurine modification defect at the first anticodon[] Finally ( viii ), we found that (like CSD) the spreading phenomenon did not cross prominent sulci (e.g., the parieto-occipital sulcus).[] See: Statistics from Introduction Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) is a major clinical entity encompassing[]

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