When Seizures Have a Genetic Cause: Understanding Epilepsy Testing
Hello everyone, November is Epilepsy Awareness Month, a time to shine a light on the millions of people worldwide living […]
Hello everyone, November is Epilepsy Awareness Month, a time to shine a light on the millions of people worldwide living […]
Genetic testing plays a crucial role in understanding autism spectrum disorder (ASD), offering insights into underlying genetic conditions that may impact health and development. While not every test provides conclusive results, genetic counselors assist families in navigating options, interpreting results, and empowering informed decisions for better care and family planning.
MKGenetix addresses the issues faced by individuals with rare connective tissue disorders, such as Ehlers-Danlos syndrome, often hindered by medical gaslighting. This phenomenon involves healthcare professionals dismissing symptoms as stress or anxiety, impacting patient confidence. Genetic counseling at MKGenetix offers validation, support, and advocacy, empowering patients in their healthcare journey.
Carrier screening is a genetic test that helps prospective parents understand their genetic background regarding inherited conditions. It’s recommended for everyone planning a pregnancy, as it empowers informed decisions. Genetic counseling aids in interpreting results and exploring reproductive options. MKGenetix offers personalized support for this important journey.
Sickle cell anemia is a hereditary blood disorder affecting hemoglobin, leading to severe pain and other complications. Advances in genetic counseling, treatment options like gene therapy, and strong community support are improving patient management and outcomes. Organizations provide resources for education and advocacy, fostering resilience and hope for affected individuals.
Newborn screening, a vital public health initiative, enables early detection of serious, treatable conditions in infants. Recently, the federal government disbanded the advisory committee overseeing this program, jeopardizing its future. MKGenetix emphasizes the need for public awareness and action to maintain equitable access to screenings and safeguard children’s health.
MKGenetix specializes in providing personalized genetic counseling for individuals and families affected by Amyotrophic Lateral Sclerosis (ALS). The service addresses genetic risks, informs family planning, and connects patients to research opportunities while navigating emotional and psychological support challenges related to the disease. Understanding ALS’s genetic aspects empowers informed health decisions.
Ehlers-Danlos Syndrome (EDS) comprises various connective tissue disorders diagnosed through clinical evaluation and genetic testing. Genetic testing confirms specific EDS types, rules out other conditions, and refines treatment plans. It empowers patients and families by enhancing risk understanding, facilitating early intervention, and supporting family planning. Genetic counselors provide crucial guidance throughout this process.
Hypermobile Ehlers-Danlos Syndrome (hEDS) is a connective tissue disorder characterized by joint hypermobility, frequent pain, and a variety of systemic
Genetic counseling is a vital tool in personalized healthcare, providing insights into genetic risks and empowering individuals to make informed health decisions. It aids in understanding hereditary conditions, personalizes prevention strategies, and supports family planning. Additionally, it offers emotional support, enabling proactive management of health and enhancing overall well-being.