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.

Also Known As:

Syndrome, Laron; Growth Hormone Receptor Defect; Growth Hormone Receptor Deficiency; Laron Dwarfism; Laron Type Dwarfism I; Pituitary Dwarfism II; Primary GH Resistance; Primary Growth Hormone Resistance; Severe GH Insensitivity; Dwarfism II, Pituitary; Dwarfism IIs, Pituitary; Dwarfism, Laron; GH Resistance, Primary; Pituitary Dwarfism IIs; Growth Hormone Insensitivity Syndrome

Musculoskeletal Diseases: 751
- Bone Diseases: 5970
  - Developmental Bone Diseases: 156
    - Dwarfism: 1206
      - Laron Syndrome: 325
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Dwarfism: 1206
    - Laron Syndrome: 325
Endocrine System Diseases: 996
- Dwarfism: 1206
  - Laron Syndrome: 325

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Disease

Drug/Important Bio-Agent (IBA)