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31 articles for “Hereditary”
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Improved Genetic Algorithmic Rule Mistreatment Hybrid Initial Population to Resolve Travelling Salesman Drawback
Abstract: Abstract: The algorithmic genetic rule is beneficial to resolve the optimization issues. It performs genetic operators to solve optimization issues. Travelling salesman problem (TSP) may be a well-known optimization downside, but TSP is beneficial to resolve the several difficulties of science and engineering. In this paper, to determine TSP, algorithmic genetic rule is applied. An initial hybrid population is generated in an algorithmic hereditary rule. The coupling of the initial …
Published in Current Trends in Information Technology · Vol. 9, Issue 3, 2019 · pp. 46–50 Read article
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Living with Glucose-6-Phosphate Dehydrogenase Deficiency
Abstract: Glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency) is an X-linked recessive hereditary disease characterized by abnormally low levels of glucose-6-phosphate dehydrogenase, a metabolic enzyme involved in the pentose phosphate pathway, especially important in red blood cell metabolism. G6PD deficiency is the most common human enzyme defect. Individuals with this disease may exhibit non-immune hemolytic anemia in response to a number of causes, most commonly infection or exposure to certain medications or fava …
Published in Journal of Nursing Science & Practice · Vol. 6, Issue 1, 2016 · pp. 23–30 Read article
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Dentitia Praecox - A Report and Review
Abstract: Child development from conception through the first years of life is marked by many changes. Eruption of every tooth, either primary or permanent, follows a chronology corresponding to the date when it erupts into the oral cavity. Though these dates are established in literature, they are subject to small variations depending on the hereditary, endocrine, and environmental factors of an individual. The expectations about the eruption of the first teeth …
Published in Research and Reviews: A Journal of Health Professions · Vol. 1, Issue 1-3, 2011 · pp. 21–24 Read article
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A Case Report on Alport Syndrome which ends up with Allograft Rejection due to Anti-GBM Disease
Abstract: Alport syndrome (AS) is a condition which is genetically inherited and is characterized by abnormalities in the basement membrane of the kidney, ear and eye as well. It is one of the spectra of diseases representing hereditary nephritis, which inevitably leads to end-stage renal disease (ESRD). Sensorineural hearing loss (SNHL) is also a characteristic feature in AS. The hearing abnormality begins during late childhood or early adolescence and 90% of …
Published in Research and Reviews: A Journal of Medicine · Vol. 9, Issue 3, 2019 · pp. 1–4 Read article
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Prevalence of Sickle Cell Disorder in Rural Vyara of Gujarat
Abstract: Sickle cell anaemias are the most common hereditary disorders in India and pose a major health problem. The study was conducted in the population of Vyara city, taluka Vyara, district Tapi of Gujarat state, India, from July 01, 2017 to September 31, 2017. The screening was done by dithionate turbidity test. The selected people were determined, and their result was established by Hb electrophoresis. The present study was carried in …
Published in Research and Reviews : A Journal of Medical Science and Technology · Vol. 7, Issue 3, 2018 · pp. 17–20 Read article
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Schwannoma of the Superficial Peroneal Nerve in 12 year Female Child: A Case Report
Abstract: Schwannomas (or neurilemmomas) are related to hereditary disorder in some patients and arise from the neurilemmal cells in nerve sheaths as lobulated, encapsulated tumours. It is commonly found in the head region but extremely found in the deep tissues of the foot. Schwannomas are slow-growing, encapsulated tumours that can be separated surgically from the parent nerve. Occasionally, intralesional degeneration with fibrosis, haemorrhage, calcification and cystic necrosis occurs in large or …
Published in Research and Reviews: A Journal of Neuroscience · Vol. 4, Issue 2, 2014 · pp. 1–4 Read article
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A Rare Case Report on Familial Dysautonomia (Familial Dysautonomia)
Abstract: Familial dysautonomia (FD) is a genetic disorder of neurodevelopment within classification of both hereditary sensory and autonomic neuropathies, each caused by a different genetic error. IKBKAP gene is responsible for the genetic error in FD. The maintenance and development of neurons occur because there is neuropathological and clinical progression. Pathological alterations consist of decreased unmyelinated and small-fiber neurons. The clinical features reflect involvement of both sensory and autonomic neurons. Sensory …
Published in Research and Reviews: A Journal of Neuroscience · Vol. 5, Issue 1, 2015 · pp. 15–18 Read article
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Recurrent Pregnancy Loss and Thrombophilia: An insight
Abstract: By definition, thrombophilia refers to acquired and/or hereditary diseases that predispose people to venous and arterial thromboembolic events. The most common cause of death on the planet is thrombosis. Myocardial infarction and stroke are major causes of morbidity and mortality in the vascular system. The deep veins of the lower extremity are the most usually involved in venous thromboembolic events, which can lead to pulmonary emboli. Thromboembolism is the major …
Published in Research and Reviews: Journal of Oncology and Hematology · Vol. 11, Issue 2, 2022 · pp. 1–7 Read article
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Hemoglobin Electrophoresis to Identify Adult Hemoglobin and Abnormal Hemoglobin Bands
Abstract: According to National Thalassemia Welfare Society (NTWS) report, every year, around 3 to 4 lakhs babies are born with one or other form of hemoglobinopathies and around 7% of the world population is carrier of hemoglobinopathies. In India, hemoglobinopathies like thalassemia and sickle cell anemia, are one of the most common hereditary disorders and cause a major health problem. In India, incidence of sickle cell and β thalassemia differ from …
Published in Research and Reviews: Journal of Oncology and Hematology · Vol. 12, Issue 2, 2023 · pp. 1–6 Read article
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The Effect of Irsal-E-Alaq (Leech) in the Management of Varicose Vein: A Review
Abstract: The varicose vein is defined as “dilated tortuous and elongated superficial vein of lower limb. Dawali (varicose veins) is one of the commonest categories of primary venous insufficiency. In Unani system of medicine, “Dawali” is described in almost all classical books of Unani medicine, synonymous with varicose veins. Varicose veins are classified into primary and secondary types. Primary varicose veins occur more frequently, and are caused by incompetent or absent …
Published in Research & Reviews : A Journal of Unani, Siddha and Homeopathy · Vol. 4, Issue 3, 2017 · pp. 13–18 Read article
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Varicose Veins and its Management in Unani and Modern System of Medicine
Abstract: The varicose vein is defined as “dilated tortuous and elongated superficial veins of the lower limb”. Dawali (varicose veins) is one of the commonest categories of primary venous insufficiency. Varicose veins are classified into primary and secondary types. Primary varicose veins occur more frequently, and are caused by incompetent or absent valves, defective connective tissue and smooth muscle weakness in venous wall and are usually hereditary in nature. As per …
Published in Research & Reviews : A Journal of Unani, Siddha and Homeopathy · Vol. 6, Issue 2, 2019 · pp. 1–6 Read article