Related Experiment Video
Updated: Aug 30, 2025

Author Spotlight: A Focus on Standardized Salivary Gland Ultrasound Protocol in Connective Tissue Disease Research
Published on: October 13, 2023
The Genesis of Sjögren
George Aw Bruyn1, Priscilla Wong2
1Reumakliniek Lelystad, Het Ravelijn 1, 8233, Lelystad, BR, The Netherlands. gawbruyn@wxs.nl.
Swedish ophthalmologist Henrik Sjögren described a syndrome linking dry eyes, dry mouth, and arthritis. His detailed monograph led to the recognition of this new condition, now known as Sjögren's syndrome.
Area of Science:
- Ophthalmology
- Rheumatology
- Medical History
Background:
- Henrik Sjögren, a Swedish ophthalmologist, authored a comprehensive monograph in 1933.
- His work detailed a distinct group of patients presenting with keratoconjunctivitis sicca, xerostomia, and arthritis.
Purpose of the Study:
- To highlight key biographical and professional milestones of Henrik Sjögren.
- To trace the development of his research that led to the identification of a new syndrome.
Main Methods:
- Review of historical medical literature and Sjögren's original dissertation.
- Analysis of the clinical observations documented in the monograph.
Main Results:
- The monograph described a constellation of symptoms: dry eyes (keratitis sicca), dry mouth (xerostomia), and joint inflammation (arthritis).
- Sjögren's meticulous documentation provided the foundation for recognizing these interconnected symptoms as a distinct clinical entity.
Conclusions:
- Henrik Sjögren's work was pivotal in delineating a new systemic autoimmune condition.
- His research laid the groundwork for the future understanding and diagnosis of Sjögren's syndrome.
More Related Videos
Related Concept Videos
Gastritis-II: Pathophysiology
In acute gastritis, the gastric mucosa becomes swollen and red and undergoes superficial erosion. Superficial ulceration may lead to bleeding.
In chronic gastritis, persistent or repeated insults lead to chronic inflammatory changes and, eventually, thinning or atrophy of the gastric tissue.
Gastritis can stem from various causes, each...
Autoimmune Disorders
Concept and Mechanism of Autoimmune Diseases
The immune...
Nephrotic Syndrome I : Introduction
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Biological Causes of Schizophrenia
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin...
Salivary Glands and Saliva

