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 […]
All Posts
Beyond BRCA: Understanding Genetic Testing for Breast Cancer
At MKGenetix, we know that conversations about breast cancer can stir up many emotions such as fear, confusion, and sometimes
Sudden Infant Death Syndrome (SIDS): Understanding Possible Genetic and Metabolic Connections
What is SIDS? Sudden Infant Death Syndrome (SIDS) is the unexpected and unexplained death of an otherwise healthy baby under
Genetics and Autism: What Families Should Know About Testing
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.
It’s Not All in Your Head: Medical Gaslighting and Connective Tissue Disorders
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.
Understanding Carrier Screening: A guide for Couples Planning Pregnancy
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.
Living with Sickle Cell Anemia: Empowerment Through Knowledge
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.
the lifesaving values of newborn screening
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.
Pharmacogenomic Testing: Personalizing Medication for Better Outcomes
Pharmacogenomic testing assesses how genes affect individual responses to medications, enhancing personalized treatment decisions. It offers benefits like increased drug efficacy, reduced side effects, and optimized dosing. While challenges such as insurance coverage and physician education persist, PGx testing is poised to revolutionize healthcare, improving patient outcomes significantly.
Understanding ALS and the Role of Genetic Counseling
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.