Familial isolated growth hormone deficiency
- PMID: 7307312
- DOI: 10.1111/j.1399-0004.1981.tb01824.x
Familial isolated growth hormone deficiency
Abstract
A family is reported with isolated growth hormone deficiency in two children, their mother and, presumably, also in two maternal uncles and their maternal grandmother. Autosomal dominant inheritance is the best explanation. Isolated growth hormone deficiency is apparently a heterogeneous condition, including autosomal dominant, autosomal recessive as well as non-genetic diseases.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources