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| Similar words: Sjogren's Syndrome | |
| Sjogren's Syndrome Sicca Syndrome | Sjogren Syndrome | Sjogrens Syndrome | Syndrome, Sicca | Syndrome, Sjogren' | s Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | |
| Sjogren-Larsson Syndrome Sjogren Larsson Syndrome Rare syndrome of autosomal recessive inheritance characterized by ichthyosis, mental retardation, and spastic pyramidal symptoms. It is associated with a defect in fatty alcohol metabolism. | |
| Keratoconjunctivitis Sicca Sicca, Keratoconjunctivitis Drying and inflammation of the conjunctiva as a result of insufficient lacrimal secretion. When found in association with XEROSTOMIA and polyarthritis, it is called SJOGREN'S SYNDROME. | |
| Mikulicz' Disease Mikulicz Disease | Disease, Mikulicz | Disease, Mikulicz' | A chronic, benign, and usually painless inflammatory swelling of the lacrimal and salivary glands. It is considered by some to include the glandular enlargement associated with other diseases, such as Sjogren's syndrome, sarcoidosis, lupus erythematosus, etc. | |
| Herpesvirus 6, Human HBLV | Herpesvirus 6A, Human | Herpesvirus 6B, Human | Human B-Lymphotropic Virus | Human herpesvirus 6 | HHV-6 | HHV-6A | HHV-6B | B-Lymphotropic Virus, Human | B-Lymphotropic Viruses, Human | Human B Lymphotropic Virus | Human Herpesvirus 6A The type species of ROSEOLOVIRUS isolated from patients with AIDS and other LYMPHOPROLIFERATIVE DISORDERS. It infects and replicates in fresh and established lines of hematopoietic cells and cells of neural origin. It also appears to alter NK cell activity. HHV-6; (HBLV) antibodies are elevated in patients with AIDS, Sjogren's syndrome, sarcoidosis, chronic fatigue syndrome, and certain malignancies. HHV-6 is the cause of EXANTHEMA SUBITUM and has been implicated in encephalitis. | |
| Spinocerebellar Degenerations Ataxias, Hereditary | Cerebellar Ataxia, Early Onset | Cerebellar Ataxia, Late Onset | Cerebellar Degenerations, Primary | Corticostriatal-Spinal Degeneration | Marie Cerebellar Ataxia | Marinesco-Sjogren Syndrome | Marie' | s Cerebellar Ataxia A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. | |
| Reye Syndrome Reye Syndrome, Adult | Reye' | s Syndrome | Reye' | s Syndrome, Adult | Reye' | s-Like Syndrome | Reye-Johnson Syndrome | Reye-Like Syndrome | Adult Reye Syndrome | Adult Reye' | s Syndrome | Reye Johnson Syndrome | Reye Like Syndrome An acute, potentially fatal metabolic disease seen primarily in children and characterized clinically by vomiting, hypoglycemia, and confusion, which may progress to coma. Pathologic features include cerebral edema and fatty infiltration of the liver and other organs. (From Adams et al., Principles of Neurology, 6th ed, p1120) | |
| Cri-du-Chat Syndrome 5p Deletion Syndrome | Chromosome 5p- Syndrome | 5p- Syndrome | Chromosome 5 Short Arm Deletion Syndrome | Crying Cat Syndrome | Deletion of Short Arm of Chromosome 5 Syndrome | 5p Syndrome | 5p Deletion Syndromes | 5p- Syndrome, Chromosome An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-). | |
| Waardenburg's Syndrome Klein-Waardenburg Syndrome | Klein' | s Syndrome | Waardenburg-Klein Syndrome | Klein Syndrome | Klein Waardenburg Syndrome | Kleins Syndrome | Syndrome, Klein' | s | Syndrome, Klein-Waardenburg | Syndrome, Waardenburg' | s Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities. | |
| Job's Syndrome Hyperimmunoglobulin E-Recurrent Infection Syndrome | Hyper-IgE Syndrome | Hyper IgE Syndrome | Hyper-IgE Syndromes | Hyperimmunoglobulin E Recurrent Infection Syndrome | Job Syndrome | Jobs Syndrome | Syndrome, Hyper-IgE | Syndrome, Job' | s A disorder of neutrophils characterized by the presence of abnormal or absent chemotactic responses and hyperimmunoglobulinemia E. It is transmitted as an autosomal recessive trait and most cases reported have been in girls. | |
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