"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.
- 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
Below are MeSH descriptors whose meaning is more general than "Dwarfism, Pituitary".
Below are MeSH descriptors whose meaning is more specific than "Dwarfism, Pituitary".
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Below are the most recent publications written about "Dwarfism, Pituitary" by people in Profiles.
Hearing loss in children with growth hormone deficiency. Int J Pediatr Otorhinolaryngol. 2017 Sep; 100:107-113.
Effect of growth hormone on bone: bone mineral density, trabecular bone volume, and alkaline phosphatase improve or are restored in the dwarf rat treated with growth hormone. J Bone Miner Res. 1995 Jan; 10(1):127-31.