Neurological Manifestations in Sjögren Syndrome
C Lafitte
Abstract
C Lafitte
Abstract
Sjogren syndrome (SS) is a systemic autoimmune inflammatory disorder characterized by lymphocytic infiltration of exocrine glands with absent or diminished glandular secretion. The salivary and lacrimal glands are primarily involved, leading to dry eyes (xerophthalmia with keratoconjunctivitis sicca) and mouth (xerostomia). Cases of xerophthalmia and/or xerostomia were first mentioned in the late 19th and early 20th centuries. In 1933, studying these symptoms and their related manifestations, Sjogren,' the Swedish ophthalmologist, concluded that they were manifestations of a general disease. Since then, the syndrome including xerophthalmia with keratoconjunctivitis and xerostomia bears Sjogren's name.
OpenAlex reports 41 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Sjogren syndrome (SS) is a systemic autoimmune inflammatory disorder characterized by lymphocytic infiltration of exocrine glands with absent or diminished glandular secretion. The salivary and lacrimal glands are primarily involved, leading to dry eyes (xerophthalmia with keratoconjunctivitis sicca) and mouth (xerostomia). Cases of xerophthalmia and/or xerostomia were first mentioned in the late 19th and early 20th centuries. In 1933, studying these symptoms and their related manifestations, Sjogren,' the Swedish ophthalmologist, concluded that they were manifestations of a general disease. Since then, the syndrome including xerophthalmia with keratoconjunctivitis and xerostomia bears Sjogren's name.
Key concepts: Sjögren syndrome, Medicine, Dermatology, Pathology, Autoimmune disease, Disease