Laron syndrome

MONDO:0009877

Laron syndrome is a congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration.

Also known as: GH receptor deficiency, Growth Hormone Insensitivity, Growth hormone receptor deficiency, Laron syndrome, Laron-type dwarfism, complete growth hormone insensitivity, primary GH insensitivity, primary GH resistance

0 clinical trials for this condition and its sub-types, 0 tagged with Laron syndrome itself.

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Part of

↑ Autosomal recessive disease (994) ↑ Growth hormone insensitivity syndrome (6)

Including sub-types (0) Tagged with Laron syndrome (0)

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