Blood Type, Genetics, Odds for COVID-19

News Picture: Blood Type, Genetics Could Impact Odds for Severe COVID-19: StudyBy Robin Foster and E.J. Mundell
HealthDay Reporters

THURSDAY, June eighteen, 2020 — A person’s genes and blood type may well aid ascertain their odds for a nastier variety of COVID-19, should they get contaminated with the new coronavirus, a new genetics study finds.

Released online June seventeen in the New England Journal of Medicine, the investigation can help affirm previously, far more anecdotal proof that blood type was tied to much better or even worse disease.

Now a staff of European scientists have located that men and women with blood type A experienced a forty five% better hazard

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Nonketotic hyperglycinemia – Genetics Home Reference

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  • Applegarth DA, Toone JR. Glycine encephalopathy (nonketotic hyperglycinaemia) : critique and update. J Inherit Metab Dis. 200427(3):417-22. Review.

  • Applegarth DA, Toone JR. Glycine encephalopathy (nonketotic hyperglycinemia): reviews and speculations. Am J Med Genet A. 2006 Jan 15140(two):186-8.

  • Coughlin CR 2nd, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodríguez-Pombo P, Väisänen ML, Spector E, Creadon-Swindell G, Brás-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, Pérez-Cerdá C, Ugarte M, Vianey-Saban

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    Constitutional mismatch repair deficiency syndrome – Genetics Home Reference

    Constitutional mismatch fix deficiency (CMMRD) syndrome is a scarce problem that significantly improves the risk of building one or more styles of most cancers in kids and younger adults. The cancers that most generally happen in CMMRD syndrome are cancers of the (significant intestine) and rectum (collectively referred to as colorectal most cancers), brain, and blood (leukemia or lymphoma).

    Almost all men and women with CMMRD syndrome build most cancers right before age 18, usually in late childhood. The age of diagnosis varies relying on the most cancers sort brain cancers, leukemia, and lymphomas have a tendency to happen at

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    Saul-Wilson syndrome – Genetics Home Reference

    Ferreira CR, Xia ZJ, Clément A, Parry DA, Davids M, Taylan F, Sharma P, Turgeon CT, Blanco-Sánchez B, Ng BG, Logan CV, Wolfe LA, Solomon BD, Cho MT, Douglas G, Carvalho DR, Bratke H, Haug MG, Phillips JB, Wegner J, Tiemeyer M, Aoki K; Undiagnosed Diseases Network; Scottish Genome Partnership, Nordgren A, Hammarsjö A, Duker AL, Rohena L, Hove HB, Ek J, Adams D, Tifft CJ, Onyekweli T, Weixel T, Macnamara E, Radtke K, Powis Z, Earl D, Gabriel M, Russi AHS, Brick L, Kozenko M, Tham E, Raymond KM, Phillips JA 3rd, Tiller GE, Wilson WG, Hamid R, Malicdan

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    ADPEAF – Genetics Home Reference

    Autosomal dominant partial epilepsy with auditory features (ADPEAF) is an uncommon form of epilepsy that runs in families. This disorder causes seizures usually characterized by sound-related (auditory) symptoms such as buzzing, humming, or ringing. Some people experience more complex sounds during a seizure, such as specific voices or music, or changes in the volume of sounds. Some people with ADPEAF suddenly become unable to understand language before losing consciousness during a seizure. This inability to understand speech is known as receptive aphasia. Less commonly, seizures may cause visual hallucinations, a disturbance in the sense of smell, a feeling

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