In simple words: Marfan syndrome is a condition where the body's connective tissue doesn't develop properly. This can cause problems in many parts of the body, such as the heart, bones, and eyes.People with this condition may be tall and thin with long arms and legs.The severity of symptoms varies greatly.

Marfan syndrome is a genetic disorder affecting connective tissue throughout the body.It's characterized by a wide range of symptoms impacting various organ systems, including the cardiovascular system (aortic aneurysm, dissection, mitral valve prolapse), skeletal system (tall stature, long limbs, scoliosis), eyes (ectopia lentis), and skin (striae). The severity and presentation of symptoms are highly variable.

Example 1: A 16-year-old presents with tall stature, long limbs, and pectus excavatum.Echocardiogram reveals aortic root dilation.Diagnosis of Marfan syndrome is made, and the patient is referred to a cardiologist for ongoing monitoring and management., A 30-year-old woman with a family history of Marfan syndrome experiences sudden onset of severe chest pain radiating to her back.Evaluation reveals an acute aortic dissection requiring emergency surgery., A 45-year-old male patient with known Marfan syndrome is undergoing routine ophthalmologic examination.Lens dislocation is detected and managed appropriately.

Detailed family history, physical examination noting characteristic features (e.g., tall stature, long limbs, arachnodactyly, scoliosis), echocardiogram, ophthalmological exam, genetic testing (if available).

** Marfan syndrome is a complex condition requiring a multidisciplinary approach.Regular monitoring is crucial to detect and manage potential complications.The information provided is for coding purposes only and does not constitute medical advice.