MRHS full form in medical term is Marfanoid Habitus Syndrome. A slender and tall body type, long fingers & toes, and other skeletal abnormalities describe this rare genetic disorder. MRHS is occurred by mutations in the FBN1 gene, which encodes the protein fibrillin-1. It usually harms the blood vessels, eyes, heart, and skeleton.
A person with Marfan syndrome is usually thin and tall, with uneven legs, long arms, fingers, and toes. Some medications are involved in the treatment of this condition. In addition, regular checkups and diagnostics are necessary to determine progress. While some cases of MRHS require preventive surgery to normalize the aorta.
If you detect the following symptoms or features, you may consult to a healthcare provider:
Since MRHS can affect tissue all over the human body, your healthcare provider may help confirm the developing and diagnosing of a treatment plan. With an accurate treatment plan and medication, it is possible to treat MRHS.