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 […]
What is SIDS? Sudden Infant Death Syndrome (SIDS) is the unexpected and unexplained death of an otherwise healthy baby under
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.
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.
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.
MKGenetix offers genetic counseling services for families dealing with developmental delays in children, aiming to identify and understand the genetic causes. They provide personalized care, connect families to resources, and empower them through knowledge. The challenges in accessing genetic services are acknowledged, and MKGenetix provides comprehensive support, including family history assessment, genetic testing, detailed consultations, and connection to local resources.
The Centers for Disease Control and Prevention reports that 1 in 54 children in the US is diagnosed with autism. Upon receiving a diagnosis, it’s important to process emotions, educate yourself about autism, and build a care team. Creating a care plan, focusing on communication, and building a support network are crucial. Remember to address behavioral challenges, take care of yourself, plan for the future, and celebrate your child’s strengths. Additional autism support groups and resources are available for further assistance.
Autism Spectrum Disorder (ASD) presents challenges in social interaction, communication, and behaviors. Therapy options like ABA, speech, occupational therapy & medication management can help. Parent-mediated interventions are effective. Genetic counseling at MKGenetix can provide valuable insights. Various support resources are available for families. Collaboration and tailored approaches are crucial for successful outcomes.
MKGenetix provides personalized genetic counseling services for individuals and families affected by hypermobile Ehlers-Danlos Syndrome (hEDS). The condition involves joint hypermobility, skin elasticity, pain, and fatigue. Seeing a genetics specialist can help identify co-occurring conditions, personalize care, provide access to research, aid in family planning, and offer understanding. MKGenetix addresses challenges in accessing genetic services and offers comprehensive support, including family history assessment, genetic testing guidance, detailed consultations, and connection to resources.