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Descriptor English: | Werner Syndrome | ||||||
Descriptor Spanish: |
Síndrome de Werner
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Descriptor Portuguese: | Síndrome de Werner | ||||||
Descriptor French: | Syndrome de Werner | ||||||
Entry term(s): |
Pangeria de l'adulte Progeria de l'adulte Progérie de l'adulte |
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Tree number(s): |
C16.320.925 C18.452.284.960 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D014898 | ||||||
Scope note: | An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease. |
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Allowable Qualifiers: |
BL sang CF liquide cérébrospinal CI induit chimiquement CL classification CN congénital CO complications DG imagerie diagnostique DH diétothérapie DI diagnostic DT traitement médicamenteux EC économie EH ethnologie EM embryologie EN enzymologie EP épidémiologie ET étiologie GE génétique HI histoire IM immunologie ME métabolisme MI microbiologie MO mortalité NU soins infirmiers PA anatomopathologie PC prévention et contrôle PP physiopathologie PS parasitologie PX psychologie RH rééducation et réadaptation RT radiothérapie SU chirurgie TH thérapie UR urine VE médecine vétérinaire VI virologie |
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DeCS ID: | 15300 | ||||||
Unique ID: | D014898 | ||||||
NLM Classification: | QZ 50 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1967/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2013/07/08 |
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Syndrome de Werner
- Preferred
Concept UI |
M0022920 |
Preferred term | Syndrome de Werner |
Entry term(s) |
Pangeria de l'adulte Progeria de l'adulte Progérie de l'adulte |
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