"Dwarfism, Pituitary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development.
Descriptor ID |
D004393
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MeSH Number(s) |
C05.116.099.343.445 C05.116.132.358 C10.228.140.617.738.300.300 C19.297.312 C19.700.482.311
|
Concept/Terms |
Dwarfism, Pituitary- Dwarfism, Pituitary
- Pituitary Dwarfism
- Growth Hormone Deficiency Dwarfism
- Hyposomatotrophic Dwarfism
- Nanism, Pituitary
- Pituitary Nanism
- Isolated Growth Hormone Deficiency
- Isolated HGH Deficiency
- Isolated Human Growth Hormone Deficiency
- Isolated Somatotropin Deficiency
- Isolated Somatotropin Deficiency Disorder
- Dwarfism, Growth Hormone Deficiency
- Isolated GH Deficiency
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Below are MeSH descriptors whose meaning is more general than "Dwarfism, Pituitary".
Below are MeSH descriptors whose meaning is more specific than "Dwarfism, Pituitary".
This graph shows the total number of publications written about "Dwarfism, Pituitary" by people in this website by year, and whether "Dwarfism, Pituitary" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2011 | 0 | 1 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Dwarfism, Pituitary" by people in Profiles.
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Decreased lifespan in female "Munchkin" actors from the cast of the 1939 film version of The Wizard of Oz does not support the hypothesis linking hypopituitary dwarfism to longevity. Geroscience. 2022 10; 44(5):2527-2539.
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Early-onset growth hormone deficiency results in diastolic dysfunction in adult-life and is prevented by growth hormone supplementation. Growth Horm IGF Res. 2011 Apr; 21(2):81-8.
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Diverse growth hormone receptor gene mutations in Laron syndrome. Am J Hum Genet. 1993 May; 52(5):998-1005.