Laron syndrome overview: Difference between revisions
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==Overview== | ==Overview== | ||
Laron syndrome is a [[autosomal recessive]] disorder characterized by an insensitivity to [[growth hormone]] (GH), caused by a variant of the [[growth hormone receptor]]. It causes [[short stature]]. | Laron syndrome is a [[autosomal recessive]] disorder characterized by an insensitivity to [[growth hormone]] (GH), caused by a variant of the [[growth hormone receptor]]. It causes [[short stature]]. | ||
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[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Endocrinology]] | [[Category:Endocrinology]] | ||
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Revision as of 19:55, 19 September 2012
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Laron syndrome Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Laron syndrome overview On the Web |
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American Roentgen Ray Society Images of Laron syndrome overview |
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Risk calculators and risk factors for Laron syndrome overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Laron syndrome is a autosomal recessive disorder characterized by an insensitivity to growth hormone (GH), caused by a variant of the growth hormone receptor. It causes short stature.