Laron syndrome overview: Difference between revisions
Jump to navigation
Jump to search
Created page with "__NOTOC__ {{Laron syndrome}} ==Overview== ==References== {{reflist|2}} {{WH}} {{WS}} Category:Disease Category:Endocrinology" |
No edit summary |
||
| (2 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Laron syndrome}} | {{Laron syndrome}} | ||
{{CMG}} | |||
==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]]. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Latest revision as of 19:56, 19 September 2012
|
Laron syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Laron syndrome overview On the Web |
|
American Roentgen Ray Society Images of Laron syndrome overview |
|
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.