An autosomal recessive disorder characterized by short stature, defective growth hormone RECEPTOR, and failure to generate insulin-like growth factor i by growth hormone. laron syndrome is not a form of primary pituitary dwarfism (growth hormone DEFICIENCY dwarfism) but the result of mutation of the human GHR gene on chromosome 5.


Leave a message about 'Laron Syndrome'


We do not evaluate or guarantee the accuracy of any content in this site. Click here for the full disclaimer.