Marfanoid hypermobility
Marfanoid hypermobility is a medical condition characterized by an unusually large range of joint movement (hypermobility) and physical characteristics similar to those seen in Marfan syndrome. It is not a disease in itself, but rather a descriptive term used to categorize individuals who exhibit certain physical traits and symptoms.
Characteristics[edit | edit source]
Individuals with marfanoid hypermobility often exhibit a tall, slender physique, long limbs, and long, thin fingers and toes, similar to those seen in Marfan syndrome. However, unlike Marfan syndrome, marfanoid hypermobility does not typically involve the cardiovascular system.
The primary characteristic of marfanoid hypermobility is an unusually large range of joint movement. This can lead to frequent joint dislocations and chronic pain. Other symptoms can include myopia (nearsightedness), flat feet, and scoliosis (curvature of the spine).
Diagnosis[edit | edit source]
Diagnosis of marfanoid hypermobility is typically based on physical examination and medical history. Genetic testing may be used to rule out Marfan syndrome and other connective tissue disorders.
Treatment[edit | edit source]
Treatment for marfanoid hypermobility primarily involves managing symptoms. This can include physical therapy to strengthen muscles and stabilize joints, pain management, and corrective lenses or surgery for myopia.
See also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD