How to find mode of inheritance Several basic modes of inheritance exist for single-gene disorders: autosomal dominant, autosomal recessive, X-linked dominant, and X-linked recessive. However, not all genetic conditions will follow these patterns, and other rare forms of inheritance such as mitochondrial inheritance exist. Youtube video: https://lnkd.in/d9X2QWwG #nikolaysgeneticslessons
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Atypical HUS: Stopping Treatment. Patients want to know about aHUS treatment duration & risk factors https://lnkd.in/euhgzb-T Complex considerations include genetics, response to complement therapy, knowledge gaps, more.
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The eyes have it: Schizophrenia is reflected in anatomical and electrophysiological indicators in the retina, which increase with the severity of the disease and the degree of genetic predisposition https://lnkd.in/ex-zdE9z
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How to Solve Probability Problems in Genetics By studying who is affected and who is not in the family, who has mild symptoms and who has a seemingly unrelated disease, or co-morbidities; it is possible to narrow down the cause of the feature, link it to a certain chromosome or identify the mode of inheritance. Youtube video: https://lnkd.in/dPVR4uQn \#nikolays_genetics_lessons
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Do you know the importance of genetics in understanding and treating hair loss? Beyond well-known factors such as lifestyle and stress, the role of specific genes in the pathogenesis of hair loss plays a very significant role. Understanding the genetic profile of patients is a new approach to personalised alopecia management. It allows us to make better informed decisions and create personalised treatment plans, perfectly aligned with each patient's genetic profile. Follow us and discover more. #HairLoss #Alopecia #HairLossTreatment #RiskFactors #Genes #GeneticTesting #FagronGenomics #Fagron #GeneticWellness #PrecisionHealth
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#snsinstitutions #snsdesignthinking #snsdesignthinkers HEMOPHILIA Haemophilia is the hemorrhagic disorder causing bleeding due to defects in the coagulation factors. Females (XX) carry two X chromosomes. If a female carries a normal X-chromosome and a mutated X-chromosome. If the gene is recessive the female will be a carrier and will not suffer from the condition. There is a 50% chance she will pass on the mutated x chromosome to her children. Males (XY) only carry one X chromosome. If a male inherits a mutated X-chromosome he will be affected by the condition whether it is dominant or recessive.
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Learn about the scientific evidence suggesting links between electromagnetic radiation and various health issues such as brain dysfunction and genetic damage. #livingspringsretreat #CellPhoneRadiation #HealthRisks #EMRAwareness
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Toxicologist, radiobiologist (Ph.D.), a medical doctor - orthopedic surgeon (Russia). Opened for research cooperation.
Progress on the role of DNA methylation in aging and longevity https://lnkd.in/gzHJ4cuQ
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Genetic, epigenetic and environmental factors determine adult body size. Adult body size then determines, along with many other factors, how quickly you age. Check out Matt Kaeberlein on the fascinating relationship between aging and body size: https://lnkd.in/gDQJuqe8
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High blood pressure may be influenced by genetics, which means that a person's genes can play a role in their blood pressure levels. This suggests that individuals with a family history of high blood pressure may be more likely to develop the condition themselves. Understanding the genetic factors involved in high blood pressure can help healthcare professionals tailor treatment plans and interventions accordingly. #HealthAndGenetics #BloodPressure
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Are you curious about how genetics relate to patients with MDS? Find out everything you wanted to know from this recent webinar, now available on-demand! https://lnkd.in/ecQuxiiK
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