Microcephaly (Small Head Size): Causes, Symptoms, and Care Options
Microcephaly, often abbreviated as MCPH, is a medical condition characterized by an abnormally small head size in infants and young…
Metachromatic Leukodystrophy (MLD): A Guide to Understanding the Disease
Metachromatic leukodystrophy, often abbreviated as MLD, is a rare and progressive genetic disorder that affects the nervous system. This condition…
Marfan Syndrome: Causes, Symptoms, and Treatments
Marfan Syndrome, often abbreviated as MFS, is a genetic disorder that affects the body’s connective tissue. This condition can impact…
Lynch Syndrome: Understanding the Genetic Risk for Cancer
Lynch Syndrome, also known as Hereditary Nonpolyposis Colorectal Cancer (HNPCC), is a genetic condition that significantly increases the risk of…
Long QT Syndrome: A Detailed Overview of Causes, Symptoms, and Treatments
Long QT Syndrome, often abbreviated as LQTS, is a rare but potentially life-threatening heart condition that affects the electrical activity…
Krabbe Disease: Understanding the Rare Genetic Disorder (Globoid Cell Leukodystrophy)
Krabbe Disease, also known as Globoid Cell Leukodystrophy, is a rare and devastating genetic disorder that primarily affects the nervous…
Klinefelter Syndrome (XXY Chromosome Disorder): Overview, Symptoms, Diagnosis & Care
Klinefelter Syndrome, also known as XXY Chromosome Disorder, is a genetic condition that affects males. It occurs when a male…
Intellectual Disability: Causes, Symptoms, and Support
Intellectual disability, often abbreviated as ID, is a condition characterized by significant limitations in both intellectual functioning and adaptive behavior….
Huntington’s Disease (HD): A Complete Guide to Understanding the Disorder
Huntington’s Disease, often abbreviated as HD, is a progressive and debilitating neurological condition that affects thousands of individuals worldwide. This…
Hunter Syndrome: Understanding the Rare Genetic Disorder (Mucopolysaccharidosis II)
Hunter Syndrome, also known as Mucopolysaccharidosis II or MPS II, is a rare and life-altering genetic disorder that primarily affects…