Genetic Diseases

Genetic Tinnitus Explained: Causes, Risks & Actions

Genetic tinnitus accounts for about one‑third of severe cases, yet noise exposure, age and health habits remain biggest triggers.

Glucose‑galactose malabsorption: What you need to know

Glucose galactose malabsorption causes diarrhea, dehydration and growth failure. Symptoms, diagnosis and diet treatment options.

Medicare genetic testing: coverage, limits, and what to expect

Medicare genetic testing covers DNA tests that guide diagnosis, treatment or drug choices, but not ancestry kits.

SHOX Syndrome: Understanding Growth Challenges in Kids

SHOX syndrome causes short stature and bone differences. Diagnosis and hormone therapy can increase height and confidence.

Is Your Personality Written in Your DNA? Let's Explore the Truth

Ever wondered if personality is genetic? Science shows half of our traits stem from DNA, while daily experiences shape the rest.

Is Noonan Syndrome Hereditary? What You Need to Know

Is Noonan syndrome hereditary? Learn how it’s inherited, the chance of new mutations, and key considerations for family planning.

Can genetics help with diagnosing and treating DMD?

Find out how genetics and DMD work together for early diagnosis, personalized care, and emerging gene‑based therapies.

Is It Possible to Change Gene Expression?

Your lifestyle choices can actually change gene expression, influencing health, mood, and aging in ways you can control.

Genes and Smell: Why You Sniff Differently Than Your Partner

Your genes shape how you experience smells, from body odor to fragrances. Find out how genetic differences affect your sense of smell.

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)

MCADD is a manageable genetic condition affecting fat metabolism. With proper care, those with MCADD can live healthy, normal lives.

Familial Mediterranean Fever: A Guide to Understanding Symptoms, Causes, and Care

Familial Mediterranean Fever causes recurring fevers and pain. Learn symptom patterns, diagnosis, and effective treatment options.

Genetic Testing for Alzheimer's: What You Need to Know

Genetic testing for Alzheimer's can provide insight into your risk. Know what the tests reveal and whether they're right for you.

Junk DNA Has Real Functions—Science Just Found Out How

Scientists are uncovering junk DNA function in gene regulation, disease, and human development—revealing ancient viral secrets within us.

Physical Therapy Exercises for Duchenne Muscular Dystrophy Management

Physical therapy involving tailored exercises can help manage Duchenne muscular dystrophy. Exercises maintain strength, flexibility, posture, cardio health and mobility.

Muscular Dystrophy Carriers: Considerations for Family Planning

Muscular dystrophy carriers can have healthy pregnancies, but should understand inheritance risks and testing options. Read on for having children as an MD mutation carrier.

Your Guide to Living Well with Muscular Dystrophy Disability

Learn how muscular dystrophy leads to disability and get tips on mobility aids, home modifications, exercise, diet, and more for improving quality of life.

Duchenne Muscular Dystrophy Awareness - Symptoms, Research & Support

Duchenne muscular dystrophy is a progressive genetic disorder. Learn about symptoms, treatment, and research during Duchenne Awareness Month in September.

Understanding Genetic Testing for Muscular Dystrophy Carriers

Genetic screening determines if you carry mutations that cause muscular dystrophy, empowering family planning and access to assisted reproductive technologies.

Essential Questions and Answers About Duchenne Muscular Dystrophy

Learn the key facts about Duchenne MD causes, inheritance, progression, emerging treatments, supportive resources, and financial help to empower informed management.

Occupational Therapy for Duchenne Muscular Dystrophy Patients

Occupational therapy helps maximize function and quality of life for Duchenne muscular dystrophy patients through skill building, adaptive equipment, accessibility modifications.

Physical Therapy Exercises and Activities for Spinal Muscular Atrophy Patients

Customized physical therapy programs with stretching, strengthening, weight bearing, balance and cardio exercises can greatly benefit SMA patients. Tips to make exercise fun.

Physiotherapy Management for Muscular Dystrophy Patients - Exercises and Treatment

Physiotherapy helps muscular dystrophy patients maintain strength, mobility and function through exercises, stretching, braces, mobility aids and lifestyle training.

Understanding Hypertrophic Calf Muscles: Causes and Symptoms

Learn about conditions like muscular dystrophy and metabolic myopathies that can cause enlarged, hypertrophic calf muscles. Key signs include muscle weakness and mobility issues.

Parenting a Child with Duchenne Muscular Dystrophy: Challenges and Hope

From an initial diagnosis to losing abilities over time, parenting a child with Duchenne MD confronts grief and caregiving burdens. Still, support and hope persist.