Answer:
Marfan syndrome is related to autosomal dominant condition.
Explanation:
There are several organs constructed of elastic fibres.
Skin, skeletons, and joints are the most frequent organs. Marfan syndrome will show as the chest form, long as well as thin bones (arms, legs, fingers), stretch marks inside the skin, or lens of the eye.
Describe Marfan Syndrome.
Marfan syndrome, the genetic illness, affects connective tissue, or even the fibres that hold and attach the organs as well as other body parts. Marfan syndrome most usually affects the skeleton, blood vessels, heart, and vision.
It occurs since the normal growth of connective tissue cannot continue with just one functional copy of such FBN1 gene.
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