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Laron dwarfism
(redirected from Laron syndrome)

   Also found in: Wikipedia 0.02 sec.
Laron dwarfism
[lä·rôN′]
Etymology: Zvi Laron, Israeli endocrinologist, b. 1927
an autosomal-recessive syndrome of skeletal growth retardation resulting from impaired ability to synthesize insulin-like growth factor I, usually because of growth hormone receptor defects. Also called Laron's syndrome.

Laron dwarfism
Genetics An AR condition characterized by target resistance to the action of hGH, due to a defect in the hGH receptor Clinical Consanguinity, severe growth retardation Lab ↑ IGF-I


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floresiensis fossils exhibit 33 skeletal symptoms of Laron syndrome, a type of insensitivity to growth hormones.
Miniature humans whose prehistoric remains were recently unearthed on an Indonesian island may have had a genetic disease known as Laron syndrome.
There is currently no approved treatment available for growth deficiency due to Laron syndrome.
 
 
 
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