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Larons syndrom
Hierarki: | ∟ ∟ ∟ Larons syndrom 6 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Larons syndrom 6 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Larons syndrom 6 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Anmärkning: | Dwarfism (1976-2004) | Growth Hormone (1976-2004) | Receptors, Cell Surface (1976-2004) | Receptors, Somatotropin (1991-2004)X |
Anmärkning: | 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 (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5.
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historyNote*: | 2005
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publicMeSHNote*: | 2005
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activeMeSHYear*: | |
dateCreated*: | 2004-07-07X |
dateEstablished*: | 2005-01-01X |
dateRevised*: | 2005-06-30X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | lktX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Laronin oireyhtymä (fi) XLaronin syndrooma (fi, ersatt) GH-överkänslighet (sv, ersatt) Laron Syndrome (en) Severe GH Insensitivity (en, ersatt) Primary Growth Hormone Resistance (en, ersatt) Primary GH Resistance (en, ersatt) Growth Hormone Receptor Defect (en, ersatt) Laron Dwarfism (en, ersatt) Laron Type Dwarfism I (en, ersatt) Growth Hormone Insensitivity Syndrome (en, ersatt) |
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