Significance of Genetic Condition
A genetic condition encompasses inherited disorders that can elevate the risk of proteinuria, including hereditary nephritis. These conditions are passed down through families and can affect kidney function, leading to protein leakage in the urine. Understanding genetic conditions is critical for identifying individuals at higher risk and ensuring appropriate monitoring and management strategies are in place to mitigate potential health complications related to kidney issues.
Synonyms: Genetic disorder, Hereditary condition, Inherited disease, Congenital condition, Hereditary disorder, Congenital disorder
The below excerpts are indicatory and do represent direct quotations or translations. It is your responsibility to fact check each reference.
Hindu concept of 'Genetic Condition'
In Hinduism, the concept of Genetic Condition may reflect concerns on consanguinity, where marrying within close relatives can escalate the risk of autosomal recessive health issues, emphasizing the importance of genetic awareness in relationships.
From: Journal of Ayurveda and Integrated Medical Sciences
(1) The study reveals that autosomal recessive conditions are strongly associated with consanguinity, potentially leading to health issues.[1]
From: International Research Journal of Ayurveda and Yoga
(1) Sickle cell anemia is a red blood cells type that does not supply oxygen in the body to healthy red blood cells.[2]
The concept of Genetic Condition in scientific sources
Genetic Condition encompasses inherited disorders like hereditary nephritis, which elevate the risk of proteinuria, indicating a connection between genetics and susceptibility to certain health issues related to kidney function.
From: South African Family Practice
(1) These health issues, such as Down’s syndrome, were studied, but genetics was not considered a major component of the curriculum for medical students during a specific period.[3] (2) These are disorders caused by abnormalities in the genes, and education about the risks of and available testing for these is important, and the study highlights the benefits and value of genetic counselling, particularly within specialist clinics.[4]
From: South African Journal of HIV Medicine
(1) NF 1 forms part of the neuro-cutaneous syndromes or phakomatoses, a group of genetic conditions predominantly involving tissues of ectodermal origin.[5]
From: Asian Journal of Pharmaceutics
(1) Sickle cell disease is marked by abnormal sickle-shaped red blood cells, which triggers vaso-occlusion, disrupting blood flow in narrow vessels.[6]
From: International Journal of Environmental Research and Public Health (MDPI)
(1) A disease or disorder that is inherited or caused by changes in genes, with a suggested relationship between prenatal exposure and the development of “idiopathic” partial androgen insensitivity syndrome.[7] (2) Genetic conditions like xeroderma pigmentosum, Fanconi’s anemia, and ataxia-telangiectasia increase the risk of oral cancer due to deficits in DNA repair mechanisms.[8]
From: Sustainability Journal (MDPI)
(1) Genetic condition of captive lions and their genetic relationship to wild populations is not well known.[9]