 Dwarfism, Pituitary
"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
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| 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 |
|---|
| 2013 | 0 | 1 | 1 | | 2017 | 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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Muus JS, Weir FW, Kreicher KL, Bowlby DA, Discolo CM, Meyer TA. Hearing loss in children with growth hormone deficiency. Int J Pediatr Otorhinolaryngol. 2017 Sep; 100:107-113.
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Matthews MA, Adler BH, Arnold MA, Kumar S, Carvalho R, Besner GE. Diffuse intestinal ganglioneuromatosis in a child. J Pediatr Surg. 2013 May; 48(5):1129-33.
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Chua SC, Hennessey K, Zeitler P, Leibel RL. The little (lit) mutation cosegregates with the growth hormone releasing factor receptor on mouse chromosome 6. Mamm Genome. 1993; 4(10):555-9.
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