The mutation of FBN1 gene results in development of condition known as Marfanoid-Progeroid-Lipodystrophy syndrome. it is also known as progeroid Fibrillinopathy. The condition is characterized by progeroid facies, few signs and symptoms of Marfan’s disease, and severe lipodystrophy. In addition, loss of lean tissue gives ‘skinny’ appearance to the patient.