Spinal Muscular Atrophy – Diagnosis & Treatments

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,

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

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

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

Spinal muscular atrophy is a progressive neurodegenerative condition. This rare genetic disease is often triggered by mutations or alterations in the genes that produce proteins required for motor neuron function.

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.

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

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