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
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Laron dwarfism. : Laron syndrome - from man to mouse : lessons from clinical and experimental experience / Zvi Laron, J. Kopchick (editors)
2011
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Laron dwarfism -- Treatment : Laron syndrome - from man to mouse : lessons from clinical and experimental experience / Zvi Laron, J. Kopchick (editors)
