Marfan Syndrome

Marfan syndrome is a genetic disorder that affects the connective tissues in the body. It is named after Antoine Marfan, the French pediatrician who first described the condition in 1896. This syndrome can affect various parts of the body, including the skeleton, eyes, heart, and blood vessels. One of the most noticeable features of Marfan... Continue Reading →

Rett syndrome

Rett syndrome is a rare genetic disorder that primarily affects girls. It was first described by Austrian physician Andreas Rett in 1966. This neurological condition is typically caused by mutations in the MECP2 gene, which is involved in the regulation of other genes. Girls with Rett syndrome usually appear to develop normally in their first... Continue Reading →

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