Search
growth hormone deficiency isolated type 1A; pituitary dwarfism I (IGHD1A)
Genetics:
- autosomal recessive
- associated with defects in GH1
Clinical manifestations:
- short stature, severe dwarfism
Laboratory:
- serum growth hormone is absent
Complications:
- patients often develop anti-GH antibodies when given exogenous GH
General
hyposomatotropism (growth hormone deficiency)
genetic disease of the endocrine system
Database Correlations
OMIM 262400
References
OMIM :accession 262400