Triple H syndrome: a novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary adrenal axis

J Clin Endocrinol Metab. 2000 Aug;85(8):2644-8. doi: 10.1210/jcem.85.8.6753.

Authors

I S Farooqi¹, M K Jones, M Evans, S O'Rahilly, J R Hodges

Affiliation

¹ University Department of Medicine, Addenbrooke's Hospital, Cambridge, United Kingdom. sorahill@hgmp.mrc.ac.uk

PMID: 10946860
DOI: 10.1210/jcem.85.8.6753

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Adrenocorticotropic Hormone / deficiency*
Adult
Alopecia Areata / physiopathology*
Autoimmune Diseases / physiopathology*
Female
Hippocampus / abnormalities*
Hippocampus / pathology
Humans
Hypothalamo-Hypophyseal System / physiopathology*
Magnetic Resonance Imaging
Memory Disorders / physiopathology
Pituitary-Adrenal System / physiopathology*
Syndrome
United Kingdom
White People

Substances

Adrenocorticotropic Hormone