At a Glance Monogenic obesity can result from rare mutations in the leptin gene usually resulting in congenital leptin deficiency which can be treated with the human leptin analogon metreleptin. Recently young children have presented with severe obesity and typical signs of leptin deficiency and high leptin levels, which is unusual, which led researchers to discover mutated leptin which was secreted but was bioinactive since it did not bind to receptors as it should.