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35 Possible Causes for POLDS

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  • Ovarian Dysgenesis

    POLD is a rare cause of adult-onset leukodystrophy presenting with dementia.[ncbi.nlm.nih.gov] The complete phenotype, genotype and pathogenetic mechanisms in POLD have not been elucidated.[ncbi.nlm.nih.gov] We followed for 18 years a woman with autopsy-proven POLD, who presented with 'frontal' dementia and spasticity.[ncbi.nlm.nih.gov]

  • Human Immunodeficiency Virus

    pold .* weights(2) envd .* weights(3); Note that different metrics were used in the calculation of the pairwise distances.[mathworks.com] […] seqpdist(aapol, 'method' , 'Jukes-Cantor' , 'indel' , 'pair' ); poltree seqlinkage(pold, 'WPGMA' ,data(:,1)) plot(poltree, 'type' , 'angular' ); title( 'Immunodeficiency[mathworks.com] A consensus tree can be built using a weighted average of the three trees. weights [sum(gagd) sum(pold) sum(envd)]; weights weights / sum(weights); dist gagd .* weights(1)[mathworks.com]

  • Cestoda

    […] established new markers from nuclear protein-coding genes for RNA polymerase II second largest subunit (rpb2), phosphoenolpyruvate carboxykinase (pepck) and DNA polymerase delta (pold[ncbi.nlm.nih.gov]

  • Taenia Solium

    However, nucleotide sequencing of a nuclear DNA gene, DNA polymerase delta (pold) revealed that all the tapeworms identified as T. asiatica using mtDNA had T. saginata type[ncbi.nlm.nih.gov] […] allele at pold locus, demonstrating that they are not "pure T. asiatica" but the hybrid descendants between the two species, confirming the wide distribution of hybrids of[ncbi.nlm.nih.gov]

  • Guanethidine

    ., Krishna, N. and Leo. pold T. H.: Ocular effects of guanethidine and its use in Glaucoma. Symposium on Guanethidine, CIBA (1960). 9. Kuchle, H.[ijo.in]

  • Infantile Neuroaxonal Dystrophy 1

    […] α-N-acetylgalactosaminidase (α-NAGA) deficiency) Neuroaxonal leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) Familial pigmentary orthochromatic leukodystrophy (POLD[clinicalgate.com]

  • Infantile Symmetrical Thalamic Degeneration

    […] α-N-acetylgalactosaminidase (α-NAGA) deficiency) Neuroaxonal leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) Familial pigmentary orthochromatic leukodystrophy (POLD[clinicalgate.com]

  • Mandibular Hypoplasia - Deafness - Progeroid Syndrome

    […] disease MDPL mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Location 19q13.33 Physical location : 50.887.592 - 50.921.270 Synonym symbol(s) POLD[genatlas.medecine.univ-paris5.fr] POLD1 is also known as CDC2, MDPL, POLD, and CRCS10), is 34 kb long, the precise location, in the GRCh38. p2 assembly, is from base pair 50,384,290 to base pair 50,418,018[wikivisually.com]

  • Leukodystrophy

    […] adult-onset leukodystrophy w/ neuroaxonal spheroids & pigmented glia; may include hereditary diffuse; pigmentary type of orthochromatic leukodystrophy w/pigmented glia (POLD[ncbi.nlm.nih.gov]

  • Idiopathic CD4 Lymphocytopenia

    Nested PCR to detect HIV-2 pol sequences in PBMCs from the patient was performed similarly, except that the primer set used was polA, polB, polC, and polD ( Table 3 ), which[nejm.org]

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