Marfan syndrome is a genetic disorder that affects the body's connective tissue, which provides support and structure to various tissues and organs. This condition is caused by mutations in the FBN1 gene, which encodes a protein called fibrillin-1. Individuals with Marfan syndrome may experience a range of symptoms, including tall stature, long limbs, joint hypermobility, and cardiovascular issues such as aortic aneurysms. Treatment typically focuses on managing symptoms and monitoring for potential complications.
marphans syndrome.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
Stockholm syndrome.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
XXXY Syndrome and Barr-Shaver-Carr Syndrome are the same.
Cushing's Syndrome
Disorders, such as Down's Syndrome, are caused by nondisjunction.
what is kinefelter syndrome?
yes there is.
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
also known as Martin-Bell syndrome, Marker X syndrome, and FRAXA syndrome
no