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laron syndrome		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 but the result of mutation of the human GHR gene on chromosome 5. [ Articles | Books | Images | Discussion groups ]
Additional comments : (Growth Hormone Insensitivity Syndrome, Laron Dwarfism)

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