Johns Hopkins Medicine’s Post

While heredity can play a role in some medical issues, appendicitis is generally caused by the appendix becoming blocked, which can be caused by a stool blockage, infection, or inflammation. These factors are less likely to be caused by heredity or genetics. Familial Patterns: Although familial clusters of appendicitis may occur in rare circumstances, it is frequently difficult to trace these occurrences purely to genetics. Understanding the complexity of appendicitis equips us with knowledge and awareness as we confront it. Consult your doctor if you have any concerns or a family history of appendicitis. Let us remain educated and prioritise our health. #AppendicitisAndGenetics #Appendicitis #Genetics #HEredity #HealthMatters #WellnessJourney #DrMaran #SpringfieldWellnessCentre

👩⚕️Researchers led by Dr. Anne Peery suggest tissue remodeling is a primary mechanism for the development of colonic diverticulitis, a debilitating gastrointestinal condition. This study aimed at identifying the determinants underlying colonic diverticulosis and the relationship with other gastrointestinal disorders. The study found that diverticulosis severity has a positive correlation with genetic predisposition to diverticulitis. 🔗 https://ow.ly/EFk650Rmp12 . . . #UNCDeptOfMedicine #ColonicDiverticulitis #GastrointestinalConditions #MedicalResearch #GastrointestinalResearch #ResearchStudy

Endometriosis has been confirmed as a hereditary disease, with the risk of developing the condition significantly higher in first-degree relatives of affected patients. Dr. Haverland recently discussed the hereditary implications of endometriosis in an article for iCareBetter. A complex disease already, the research and understanding of the genetics and epigenetics of endometriosis continues to require more research! 🎗️ Familial endometriosis may be more severe than sporadic cases. This also supports the multifactorial inheritance of endometriosis and a genetic propensity as it may spread more severely to offspring or siblings. 🎗️ The genetic/epigenetic theory suggests that the treatment of endometriosis should focus on the complete excision of the lesions to prevent recurrence Click the link in bio to read the full article. At PRM, we want patients to know that pain is never normal. You deserve to be heard and you deserve your pain to be taken seriously and to be healed. 💜

Rare Disease Day: read Tiff's story about taking part in genetics research to help people with conditions like her https://lnkd.in/e53AsQ6V Learn more about taking part in research and search for studies at https://lnkd.in/dfYFj7hR

Spinal diseases can be caused by genetic factors. Conditions such as scoliosis can be associated with family history. Some spinal diseases are associated with specific genetic traits or mutations. However, genetic predisposition is only one factor, and environmental factors, lifestyle, and other factors also affect spinal health. Therefore, it is thought that genetic and environmental factors work together in the development of spinal diseases. #osimplant #spinesurgery #spinehealth #health #spine #implant #spineimplant

Aaron Besterman, RCIGM Principal Investigator, looks at a genetics-guided approach to the clinical management of schizophrenia. His review discusses how genetics informs schizophrenia management and outlines future research areas with potential impacts. It also emphasizes ethical concerns, including healthcare disparities and unintended consequences of genetic technologies in clinical practice. Read the full publication : https://lnkd.in/gs4f_RWT #genomics #WholeGenomeSequencing #raredisease #schizophrenia

📣 In reality, rare diseases are anything but! Worldwide, they affect 260 to 450 million patients.   ⬇️ Nicolas Levy, physician and researcher in medical genetics and Chief Scientist Rare Diseases at Servier, explains the major challenges of research in rare diseases in the latest issue of Insights by Servier.   💪 At Servier, our goal is to meet patients’ medical needs and improve their quality of life. For example, we are focusing our R&D efforts on discovering new medicines that slow the progression of diseases with a genetic origin, which is the case for more than 80% of rare diseases.   Read Nicolas Levy’s full interview on rare diseases at 👉 https://lnkd.in/eBTC-jga   #WeAreServier #InsightsByServier #RareDiseases

The Huntington's Disease Association is delighted to welcome Consultant Clinical Geneticist Nayana Lahiri for this webinar on the genetics of Huntington's disease. Nayana will be talking about the genetics basis of Huntington's disease answering questions such as: What does CAG repeat mean? What about the risk to other family members? Nayana will be discussing how understanding the genetics of Huntington's disease helps families- looking at topics such as family planning options and the development of potential therapies. https://loom.ly/RCSFqZI

Another Friday means more health-related findings. The first article looks at a new treatment for patients with cystic fibrosis, which has succeeded in achieving long-lasting modifications. https://lnkd.in/gYVFuu6V The second article focuses on a new study that has identified more than 140 novel genetic risk factors associated with the development of restless legs syndrome. https://lnkd.in/ghQQNEDu The final article examines how a single network in the brain may be responsible for stuttering. https://lnkd.in/g_nG3qqq #manhattanlife #healthscience #medicalscience #healthfindings