Results 1 -
10
of
10
for
Marfan syndrome OR hyperextensibility symdrome OR arachnodactyly
- ... Milewicz DM. FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly. J Med Genet. 2004 May;41(5):e56. ...
- ... Milewicz DM. FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly. J Med Genet. 2004 May;41(5):e56. ...
- Marfan Syndrome (National Library of Medicine)Marfan syndrome is a disorder that affects connective tissue. Connective tissues are proteins that support skin, bones, blood vessels, and other organs. One ...
- ... those of people with a genetic condition called Marfan syndrome. For example, they may have long, slender fingers (arachnodactyly), unusually long limbs, a sunken chest (pectus excavatum) ...
- Causes may include: Homocystinuria Marfan syndrome Other rare genetic disorders
- ... as skipped or extra beats (palpitations).Individuals with Marfan syndrome are usually tall and slender, have elongated fingers and toes (arachnodactyly), loose joints, and have an arm span that ...
- People with Marfan syndrome are often tall with long, thin arms and legs and spider-like fingers (called arachnodactyly). The length of the arms is greater than height when arms are stretched out. Other symptoms include: A ...
- Beals Syndrome (Marfan Foundation)Marfan Syndrome/Related Issues ... Marfan Syndrome ... Marfan Foundation ... Like Marfan, beals syndrome affects the body's connective tissues, however, beals can also ...
- Connective Tissue Disorders (National Library of Medicine)... types: Genetic disorders, such as Ehlers-Danlos syndrome, Marfan syndrome, and osteogenesis imperfecta Autoimmune disorders, such as lupus ...
- ... affected. Homocystinuria has several features in common with Marfan syndrome , including skeletal and eye changes.