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Sjögren's Syndrome
Sjögren's syndrome
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Overview
Anatomy
Health Providers & Organizations
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Connective tissue diseases
Sjogren's syndrome
Meyenburg-- Altherr-Uehlinger syndrome
Mixed connective tissue disease
Erythematosus
Rheumatology
Rheumatic disorders
Scleroderma
Antiphospholipid syndrome
Sjogren's syndrome
Mixed connective tissue disease
Erythematosus
Autoimmune diseases
Autoimmune disorder
Churg-strauss syndrome
Autoantigen
Sjogren's syndrome
Meyenburg-- Altherr-Uehlinger syndrome
Antiphospholipid syndrome
Erythematosus
Syndromes
(9)
Sjogren-larsson syndrome
Keratoconj- unctivitis sicca
Massive myoclonia
Hallerman-Streiff Syndrome
Conradi syndrome
Conradi syndrome
Mowat-Wilson syndrome
Marshall-smith syndrome
Sjogren's syndrome
Antiphospholipid syndrome
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Diseases and disorders
(49)
Marinesco sjogren syndrome
Serous meningitis
Ecchymoses
Ichthyosis
Megalocornea mental retardation syndrome
Megalocornea mental retardation syndrome
Metatropic dwarfism, type II
Polymyositis
Megalencephaly with hyaline inclusion
Alpha b lysosomal mannosidosis
Maxillonasal dysplasia binder type
Myopathy desmin storage
Maxillofacial dysostosis
Neutral lipid storage disease
Myoclonic progressive familial epilepsy
Mucosulfatidosis
Xerophthalmia
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
Subacute sclerosing leukoencephalitis
major aphthous ulcer
MTP deficiency
Netherton syndrome ichthyosis
Ichthyosis hystrix curth macklin type
Cryoglobulinemia
Macular degeneration polymorphic
Mucolipidosis type 4
Megalencephaly cutis marmorata telangiectatica congenita
Oculo-gast- rointestinal muscular dystrophy
Xerostomia
Muscular dystrophies, limb-girdle
Microcephalic primordial dwarfism
Ectodermal dysplasia
Malignant atrophic papulosis
Monosaccharide malabsorption
Peeling skin syndrome
Cacchi-Ricci disease
CHILD syndrome
Melnick-needles syndrome
Keratosis follicularis spinulosa decalvans
Sjogren's syndrome
Sjogren-larsson syndrome
Keratoconj- unctivitis sicca
Massive myoclonia
Meyenburg-- Altherr-Uehlinger syndrome
Rheumatic disorders
Scleroderma
Antiphospholipid syndrome
Churg-strauss syndrome
Mixed connective tissue disease
Erythematosus
more...
Ophthalmology
Marcus Gunn jaw winking syndrome
Artificial tears
Pilocarpine
Serous meningitis
Keratoconj- unctivitis sicca
Xerophthalmia
Genetic disorders
(15)
Schilder-Addison Complex
Inherited disease
Partial monosomy 13q
Mulibrey nanism syndrome
Mitochondrial disorders
Mitochondrial disorders
Congenital ichthyosiform erythroderma
Metatropic dwarfism, type II
Megalencephaly with hyaline inclusion
Mucosulfatidosis
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
MTP deficiency
Hallerman-Streiff Syndrome
Mucolipidosis type 4
Mowat-Wilson syndrome
Monosaccharide malabsorption
more...
Symptoms
(17)
Smell impaired
Reddened skin
Arthralgia
Cloudy cornea
Dental caries
Dental caries
Dryness of the mouth
Dysphagia
Dysphonia
Fatigue
Itching eyes
Joint swelling
Loss of sense of taste
Lymphadenopathy
Rapid eye movements
Spasticity
Keratoconj- unctivitis sicca
Xerostomia
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Anti-nuclear antibody
(10)
Anti-centromere antibodies
Anti-glyco- protein-210 antibodies
Anti-nRNP
Anti-p62 antibodies
Anti-sp100 antibodies
Anti-sp100 antibodies
Anti-topoisomerase antibodies
Extractable nuclear antigens
LSm
Primary biliary cirrhosis
Anti-Ro
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Signs and tests
Rheumatoid factor
ANA
Antibodies
Oral ulcer
Salivary gland biopsy
Slit lamp examination
Tear test
See also
(20)
Semivegetarian
Single palmar crease
Scrofuloderma
Second cranial nerve
Schizophrenia, disorganized
Schizophrenia, disorganized
Senile lentigines
Fatty aldehyde dehydrogenase
Founder effect
Neurologic disorder
Congenital ichthyosiform erythroderma
Fatty alcohol
Hyperkeratosis
Heterozygotes
Glands
Salivary glands
Parotid glands
NAD+
Maxillonasal dysplasia
Genetic change
Fat restriction
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