Abstract
Acromegaly is a rare endocrine disorder occurred by an over production of growth hormone. Cause s of acromegaly include benign tumor of pituitary gland, over production of growth hormone as well as genetic predisposition. Clinical features of acromegaly are acral enlargement, prognatism, kyphosis, soft tissue as well a s facial chanjes, hyper glycemia, hypertension, hypogonadism, thyroid dysfunction and cardiomyopathy. Diagnosis is based on MRI and CT scan. Treatment is dependent on somatostatin analogs, dopamine agonists, GH receptor antagoni sts.