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MeSH 搜索器

Laron Syndrome

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.
推出的年份: 2005
副标题
树号: C05.116.099.343.679, C16.320.240.750, C19.297.656
MeSH 单一 ID: D046150
进入的组:
  • Syndrome, Laron
  • Growth Hormone Receptor Defect
  • Growth Hormone Receptor Deficiency
  • Pituitary Dwarfism II
  • Dwarfism II, Pituitary
  • Dwarfism IIs, Pituitary
  • Pituitary Dwarfism IIs
  • Laron Type Dwarfism I
  • Primary GH Resistance
  • GH Resistance, Primary
  • Primary Growth Hormone Resistance
  • Severe GH Insensitivity
  • Growth Hormone Insensitivity Syndrome
  • Laron Dwarfism
  • Dwarfism, Laron
早前的内容:
  • Dwarfism (1976-2004)
  • Growth Hormone (1976-2004)
  • Receptors, Cell Surface (1976-2004)
  • Receptors, Somatotropin (1991-2004)

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