| Literature DB >> 7002061 |
Abstract
Mendenhall's syndrome comprises insulin-resistant diabetes, pineal hyperplasia, and various somatic anomalies. A boy with this condition now aged 12 years is reported; a similarly affected sibling died aged 7.8 years. Hypophysectomy has been of short-term benefit, but the problems of insulin resistance persist. On the basis of monocyte-binding studies it seems likely that in this condition there is an inherited deficiency of insulin receptors.Entities:
Mesh:
Substances:
Year: 1980 PMID: 7002061 PMCID: PMC1627057 DOI: 10.1136/adc.55.8.619
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791