Laron Syndrome

Growth Hormone Receptor Defect; Laron Dwarfism; Laron Type Dwarfism I; Primary GH Resistance; Primary Growth Hormone Resistance; Severe GH Insensitivity; Dwarfism, Laron; GH Resistance, Primary; Syndrome, Laron
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.