What does CMD mean in BRITISH MEDICINE

CMD is caused by inherited genetic mutations that affect the structure or production of certain proteins in connective tissue. These mutations can occur spontaneously or be passed on from one generation to another through a family history of CMD.

The most common symptoms associated with CMD include enlargement of veins and arteries, high blood pressure, aneurysms, and varicose veins, as well as an increased risk for stroke and heart attack. Other signs might include chest pain, easy bruising and skin lacerations due to thinning skin. In some cases, affected individuals may also experience difficulty breathing, dizziness and fainting spells.

Diagnosis generally involves a physical examination, patient questionnaire about medical history, genetic testing to identify any mutations that may be causing CMD, imaging tests such as MRI or CT scan and other medical tests.

Treatment typically focuses on managing specific symptoms such as reducing high blood pressure or preventing potential complications like stroke or heart attack. Surgery may be necessary in some cases to repair damaged tissues in order stabilize the condition. Medications may also be prescribed to ease inflammation or relax blood vessels in order reduce pressure buildup. Physical therapy may also help improve mobility and maintain overall strength and balance.

Unfortunately there is no known cure yet for this condition; however research is ongoing into possible treatments that could provide relief or prevent further damage over time.