Causes of Spinal Muscular Atrophy

Angelman syndrome is a genetic condition that causes considerable intellectual and developmental disability, sleep problems, and movement issues. Kids with this disorder tend to have some distinctive symptoms and features. However, it can be hard to diagnose them once...

What Is Klinefelter Syndrome? Klinefelter syndrome is a common genetic disorder. It leads to abnormal developments only in males. Currently, the average time to diagnose this condition is in the mid 30s. However, many people still remain undiagnosed during their...

Spinal muscular atrophy is a rare genetic condition that can affect motor neurons in your spinal cord. This leads to weakness or deterioration of the muscles needed for movement. In most cases, symptoms tend to occur at birth or...

Spinal muscular atrophy or SMA is a genetic disease. It causes muscles to become emaciated and weak over time. Most cases can be diagnosed in young children or babies. Currently, there is still no cure for the condition. However,...

What Is Marfan Syndrome? Marfan syndrome is a genetic connective tissue condition. It would affect the usual development of the body because connective tissue plays a key role in supporting the skeletal structure and other body parts. In addition, the...

What Is Prader-Willi Syndrome? Prader-Willi syndrome is a genetic condition that can be passed from parents to their children. It is mostly present at birth, but diagnosis usually does not occur until later stages in life. People with this disorder...

Williams syndrome is a genetic condition characterized by many developmental issues. This syndrome is quite rare as it only occurs in approximately 1 in 10,000 people. A genetic link is often present in those with this health issue, but...

What Is Fragile X Syndrome? Fragile X syndrome, also called Martin-Bell syndrome, is a genetic disorder that leads to developmental and intellectual disabilities. It may be passed down to children from their mothers or fathers. It is the most common...