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Genetic Disorders

Articles on genetic disorders from TheKnowHow: awareness, prevention, diagnosis and treatment, with international expert insight.

Genetic Disorders

15 articles

Genetic Disorders31 August 2026Spinal Muscular Atrophy: Symptoms, Types and TreatmentSpinal muscular atrophy second opinion UAE: if your child has been diagnosed with SMA, an independent spinal muscular atrophy second…Read article · 5 min
Genetic Disorders30 June 2026PKU International Awareness DayPKU International Awareness Day 2026, Breaking the silence on mental health in PKU Living with a rare or chronic condition inevitably…Read article · 4 min
Genetic Disorders22 June 2026World Sickle Cell Awareness Day 2026Every Drop Matters: Supporting the Sickle Cell Community. The 19th June each year marks a milestone in the awareness activities over the…Read article · 5 min
Dermatology13 June 2026Albinism Awareness DayProudly In My Skin: Celebrating All Skin Tones The 2026 theme “Proudly in my skin, celebrating all skin tones” is also…Read article · 5 min
Genetic Disorders17 April 2026World Hemophilia Day: Understanding Bleeding DisordersWorld Hemophilia Day 2026: Advancing Equity in Care. On April 17 each year, World Hemophilia Day is celebrated worldwide to…Read article · 7 min
Genetic Disorders2 March 2026Rare Diseases in the UAE: Small Numbers, Big ImpactIndividual Rare, Collectively Common, What is a Rare Disease Rare diseases may be uncommon individually, but together they affect…Read article · 7 min
Genetic Disorders24 August 2025Rare Genetic Disorder: Awareness, Diagnosis & SupportToday, we listen to a physician and mother, reflecting on her own medical odyssey with her son diagnosed with a rare genetic conditionRead article · 4 min
Genetic Disorders20 August 2025Spinal Muscular Atrophy (SMA): Understanding a Genetic Disorder!There is no “right way” to live with a disease like SMA. Every person’s experience is different, and it’s every person’s right to decide what SMA means for them.Read article · 9 min
Genetic Disorders19 June 2025Sickle Cell DiseaseSickle cell disease is a serious inherited blood disorder that affects millions worldwide, altering the shape of red blood cells and causing lifelong health complications.Read article · 3 min
Genetic Disorders17 April 2025One World, One Voice for Hemophilia!A global community raising hemophilia awareness on World Hemophilia Day What Is Hemophilia? Hemophilia is a rare and serious congenital bleeding disorder that affects the blood’s ability to clot. As a result, people with hemophilia bleed for a longer time than normal.Read article · 6 min
Genetic Disorders21 March 2025Individuals with Down Syndrome-Different, Not Less!Down Syndrome Day, celebrated annually on March 21st, is a worldwide initiative to increase awareness and advocate for the inclusion of individuals with Down Syndrome. This genetic condition results from an extra copy of chromosome 21 and influences various aspects of health and development.Read article · 5 min
Genetic Disorders28 February 2025Shine a Light on Rare DiseasesMillions worldwide are affected by rare diseases, often beginning in childhood. While each disease is uncommon, together they impact one in ten people. Patients face a long and challenging journey, from delayed diagnoses to limited treatment options. Genetic research and international collaboration are crucial for the future of these patients and their families. Raising awareness, sharing knowledge, and offering support are key to improving the lives of those living with a rare disease.Read article · 7 min
Genetic Disorders28 August 2024Spinal Muscular Atrophy (SMA): Understanding a Genetic Disorder!Spinal Muscular Atrophy (SMA) is a rare genetic disorder that affects motor neurons, leading to progressive muscle weakness. Thanks to recent advances, new treatments now offer improved quality of life and motor abilities, especially when diagnosed early. Every family deserves information, support, and guidance throughout their care choices.Read article · 12 min
Genetic Disorders22 July 2024Fragile X Awareness DayFragile X Syndrome is the most common inherited cause of intellectual disability in children, affecting about 1 in 2,400 births. Early diagnosis and support can help maximize the potential and independence of affected children. While there is currently no cure, tailored therapies and community resources empower families to overcome challenges and foster a supportive environment.Read article · 7 min
Genetic Disorders17 July 2024Cord Blood BankingCord blood banking is a forward-thinking healthcare option that allows families to preserve the stem cells found in a newborn’s umbilical cord. These cells hold the potential to treat over 80 diseases, including blood disorders, immune deficiencies, and certain cancers. By storing cord blood, families create a biological safeguard for future medical needs and support the growth of regenerative medicine. The process is safe, minimally invasive, and offers hope for innovative therapeutic interventions.Read article · 7 min