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werner's syndrome - premature aging
Definition for Werner's Syndrome
Werner syndrome is a very rare, autosomal recessive disorder; its most recognizable characteristic is premature aging.
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Werner syndrome is a very rare, autosomal recessive disorder; its most recognizable characteristic is premature aging. Werner's syndrome more closely resembles "accelerated aging" than any other "segmental progeria." For this reason, Werner syndrome is often referred to as a progeroid syndrome, as it partly mimics the symptoms of Progeria. The defect is on a gene that codes DNA helicase and it is located on the short arm of the 8th chromosome. As a result DNA replication is impaired in this syndrome. This condition is inherited in an autosomal recessive pattern.
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some common symptoms
face deformities
muscle wasting
not gaining weight
scalp hair loss
some related diagnoses
1 - 7 of
13
diagnoses
fetal alcohol syndrome
syphilis
pituitary adenoma
hypothyroidism
multiple endocrine neoplasia type 1
multiple endocrine neoplasia type 2b
relapsing polychondritis
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do i have 'Werner's Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'werner's syndrome'
1 - 5 of
11
diagnostic tests
Follicular Stimulating Hormone (FSH)
Werner's Syndrome and Follicular Stimulating Hormone (FSH)
Glucose Tolerance Test
A test for diabetes
Werner's Syndrome and Glucose Tolerance Test
Leuteinizing hormone (LH)
Werner's Syndrome and Leuteinizing hormone (LH)
Serum T3
Werner's Syndrome and Serum T3
Serum T4 free
Werner's Syndrome and Serum T4 free
Serum TSH
Werner's Syndrome and Serum TSH
Serum Testosterone
Werner's Syndrome and Serum Testosterone
fasting lipid profile
Werner's Syndrome and fasting lipid profile
serum estradiol
Werner's Syndrome and serum estradiol
serum glucose
Werner's Syndrome and serum glucose
Developmental testing
Werner's Syndrome and Developmental testing
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therapeutic procedures for 'Werner's Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Werner's Syndrome:
therapeutic procedure search results for 'werner's syndrome'
rankings are computer generated. please consult your health care provider.
medications search results for 'werner's syndrome'
rankings are computer generated. please consult your health care provider.
web search results for werner's syndrome
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1 - 50
- Werner's Syndrome
Werner's syndrome and endocrine disorders.
Werner's syndrome was diagnosed on the basis of his characteristic clinical appearance. ... Thus, in Werner's syndrome metabolic and endocrinologic investigation is ...
http://www.ncbi.nlm.nih.gov/pubmed/12910063
www.ncbi.nlm.nih.gov
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Neurological complications of Werner's syndrome.
1174-8 Patients with Werner's syndrome have the appearance of premature ageing. ... System Diseases etiology Spinal Cord Diseases etiology pathology Werner Syndrome ...
http://www.ncbi.nlm.nih.gov/pubmed/14586597
www.ncbi.nlm.nih.gov
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Werner's Syndrome: A Rare Cause of Hoarseness.
... 2008 08 20 0892-1997 22 4 2008 Jul Werner's syndrome: a rare cause of hoarseness. 509-11 Werner's syndrome (WS) is a rare hereditary disorder which is ...
http://www.ncbi.nlm.nih.gov/pubmed/17241770
www.ncbi.nlm.nih.gov
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Cigarette smoke induces cellular senescence via Werner's syndrome ...
Both Werner's syndrome and cigarette smoking accelerate aging. ... Rescue of Werner's syndrome protein down-regulation may represent a potential ...
http://www.ncbi.nlm.nih.gov/pubmed/19011155
www.ncbi.nlm.nih.gov
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A novel protein interacts with the Werner's syndrome gene product ...
... with the Werner's syndrome gene product physically ... Werner's syndrome (WS) is a rare autosomal recessive disorder characterized by premature aging. ...
http://www.ncbi.nlm.nih.gov/pubmed/11301316
www.ncbi.nlm.nih.gov
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Positional cloning of the Werner's syndrome gene.
258-62 Werner's syndrome (WS) is an inherited disease with clinical symptoms ... RecQ Helicases Sequence Alignment Werner Syndrome genetics 1996 4 12 1996 ...
http://www.ncbi.nlm.nih.gov/pubmed/8602509
www.ncbi.nlm.nih.gov
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Werner syndrome - Wikipedia, the free encyclopedia
Werner's syndrome more closely resembles accelerated aging than any other ... The Werner syndrome protein ... linkage of Werner's syndrome to five markers ...
http://en.wikipedia.org/wiki/Werner_syndrome
en.wikipedia.org
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Disorders of Accelerated Aging: The Aging Body: Merck Manual Home Edition
In Hutchinson-Gilford syndrome and Werner's syndrome, the central nervous system ... Werner's Syndrome: This hereditary syndrome begins in adolescence or early adult ...
http://www.merck.com/mmhe/sec01/ch003/ch003e.html
www.merck.com
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Smokers Have Rapid Aging Defect - MedicineNet - Health and Medical ...
Read doctor-produced health and medical information written for you to make informed ... Werner's syndrome is caused by a mutation in a gene called WRN. ...
http://www.medicinenet.com/guide.asp?s=rss&k=DailyHealth&a=97518
www.medicinenet.com
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Werner syndrome - Genetics Home Reference
Werner syndrome is characterized by the dramatic, rapid appearance of features ... Many people with Werner syndrome have thin arms and legs and a thick trunk due ...
http://ghr.nlm.nih.gov/condition=wernersyndrome
ghr.nlm.nih.gov
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Werner Syndrome - Yahoo! Health
Important It is possible that the main title of the report Werner Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ...
http://health.yahoo.com/other-other/werner-syndrome/healthwise--nord135.html
health.yahoo.com
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Bones, muscles, and connective tissues - Genetics Home Reference
Werner syndrome. Westphall disease see hypokalemic periodic paralysis ... WS see Werner syndrome; Williams syndrome. WZS see Weissenbacher-Zweymüller syndrome ...
http://www.ghr.nlm.nih.gov/conditionCategory=bonesmusclesandconnectivetissues
www.ghr.nlm.nih.gov
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Werner syndrome ATP-dependent helicase - Wikipedia, the free encyclopedia
WRN (Werner syndrome) is a human gene ... The Werner syndrome protein at the crossroads of DNA repair and apoptosis" ... Werner Syndrome Mutational Database ...
http://en.wikipedia.org/wiki/Werner_syndrome_ATP-dependent_helicase
en.wikipedia.org
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WRN - Werner syndrome - Genetics Home Reference
The official name of this gene is "Werner syndrome." WRN is the gene's official symbol. ... Werner syndrome - caused by mutations in the WRN gene ...
http://ghr.nlm.nih.gov/gene=wrn
ghr.nlm.nih.gov
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THE MERCK MANUAL OF GERIATRICS, Index W
Wallenberg's syndrome 1031. Wandering 371. Ward 131 ... Werner's syndrome 8. Wernicke's aphasia 424t, 428. Wernicke's encephalopathy 335, 338 ...
http://www.merck.com/mkgr/mmg/index/ind_w.jsp
www.merck.com
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Human WRN (Werner's syndrome) related family member (wrn-1) (wrn-1) (wrn-1)
Nematode protein-coding gene wrn-1. Represented by 24 ESTs from 7 cDNA libraries. ... Caenorhabditis elegans human WRN (Werner's syndrome) related family member (wrn ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Cel&CID=7245
www.ncbi.nlm.nih.gov
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Genomics|HuGENet|e-Journal|Longevity & CETP
The mission of the National Office of Public Health Genomics is to integrate advances in human genetics into ... between the Werner syndrome helicase and ...
http://www.cdc.gov/genomics/hugenet/ejournal/lipoprotein.htm
www.cdc.gov
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Life span elongation of Werner's syndrome fibroblasts by co-culture ...
Life span elongation of Werner's syndrome fibroblasts by co-culture with origin ... of late-phase-II fibroblasts from patients with Werner's syndrome (WS cells) ...
http://www.ncbi.nlm.nih.gov/pubmed/6094336?dopt=Abstract
www.ncbi.nlm.nih.gov
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Werner syndrome - References - Genetics Home Reference
Gene Review: Werner Syndrome ... of WRN mutations in Werner syndrome patients. ... Pathways and functions of the Werner syndrome protein. Mech Ageing Dev. ...
http://ghr.nlm.nih.gov/condition=wernersyndrome/show/References
ghr.nlm.nih.gov
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THE MERCK MANUAL OF GERIATRICS, Ch. 1, Biology of Aging
Werner's syndrome produces sclerodermal skin changes and baldness, which make ... The gene involved in Werner's syndrome codes for a DNA helicase, an enzyme that ...
http://www.merck.com/mkgr/mmg/sec1/ch1/ch1e.jsp
www.merck.com
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WebMD Health A-Z - Find reliable health and medical information on ...
Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable ... WS -- Werner Syndrome. WSS. Health A-Z ...
http://www.webmd.com/a-to-z-guides/health-topics/wp-wt.htm
www.webmd.com
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Eyes and vision - Genetics Home Reference
Werner syndrome. Whitnall-Norman syndrome see Norrie disease ... WS see Werner syndrome. X-ALD see X-linked adrenoleukodystrophy. X-linked adrenoleukodystrophy ...
http://ghr.nlm.nih.gov/conditionCategory=eyesandvision
ghr.nlm.nih.gov
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Progeria: Miscellaneous Disorders in Infants and Children: Merck Manual ...
... progeroid syndromes, including Werner's syndrome (premature aging after puberty ... Cockayne syndrome is an autosomal recessive disease caused by mutation in the ...
http://www.merck.com/mmpe/print/sec19/ch286/ch286d.html
www.merck.com
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Smokers Have Rapid Aging Defect
Cigarette smoke causes the same cellular defect seen in people with Werner's syndrome -- a rare genetic disease that makes people age very fast.
http://www.webmd.com/smoking-cessation/news/20090206/smokers...
www.webmd.com
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Cancer - Genetics Home Reference
Gorlin syndrome. hereditary leiomyomatosis and renal cell cancer. hereditary multiple exostoses ... Rubinstein-Taybi syndrome. tuberous sclerosis. Werner syndrome ...
http://ghr.nlm.nih.gov/conditionGroup=cancer
ghr.nlm.nih.gov
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Genetic Disease on MedicineNet.com
Learn more about the field of genetics and the future possibility of ... years, Martin has been studying Werner's syndrome, a disease that causes people ...
http://www.medicinenet.com/script/main/art.asp?articlekey=51444
www.medicinenet.com
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Encyclopedia W-Wz on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, ... Werner Syndrome. Wernicke-Korsakoff Syndrome. West Nile Encephalitis ...
http://health.yahoo.com/ency/w
health.yahoo.com
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Werner syndrome
Provides a short descriptions of the inherited disorder, Werner syndrome. ... The molecular role of WRN in Werner syndrome therefore remains to be proven, as ...
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..Show...
www.ncbi.nlm.nih.gov
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Chromosome 8 - Conditions related to genes on chromosome 8 - Genetics ...
CHARGE syndrome. Cohen syndrome. color vision deficiency ... Rothmund-Thomson Syndrome. spastic paraplegia type 8. Waardenburg syndrome. Werner syndrome ...
http://ghr.nlm.nih.gov/chromosome=8/show/Conditions
ghr.nlm.nih.gov
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Werner Syndrome -- GeneReviews -- NCBI Bookshelf
Werner syndrome is characterized by the premature appearance of features ... Individuals with Werner syndrome develop normally until the end of the first decade. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=werner
www.ncbi.nlm.nih.gov
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Skin, hair, and nails - Genetics Home Reference
Adult premature aging syndrome see Werner syndrome. Adult Progeria see Werner syndrome ... Bloch-Siemens syndrome see incontinentia pigmenti ...
http://ghr.nlm.nih.gov/conditionCategory=skinhairandnails
ghr.nlm.nih.gov
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277700
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277700
www.ncbi.nlm.nih.gov
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Adult Soft Tissue Sarcoma
Adult soft tissue sarcoma is a disease in which malignant (cancer) cells form in ... Li-Fraumeni syndrome. Werner syndrome. Basal cell nevus syndrome. ...
http://www.webmd.com/cancer/tc/ncicdr0000258102-general-info...
www.webmd.com
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WRN - References - Genetics Home Reference
Werner syndrome protein: functions in the response to DNA damage ... Comai L, Li B. The Werner syndrome protein at the crossroads of DNA ... Werner ...
http://ghr.nlm.nih.gov/gene=wrn/show/References
ghr.nlm.nih.gov
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Werner syndrome (WRN)
Human protein-coding gene WRN. Represented by 70 ESTs from 57 cDNA libraries. ... Werner syndrome (WRN) SELECTED PROTEIN SIMILARITIES ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=632050
www.ncbi.nlm.nih.gov
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Index: WE: Merck Manual Professional
Wermer's syndrome. Conditions Associated With MEN Syndromes ... Werner's syndrome. Progeria. Wernicke-Korsakoff syndrome. Thiamin: Symptoms and Signs ...
http://www.merck.com/mmpe/index/ind_we.html
www.merck.com
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Werner syndrome homolog (human) (Wrn)
Mouse protein-coding gene Wrn. Represented by 81 ESTs from 54 cDNA libraries. ... Mus musculus Werner syndrome homolog (human), mRNA (cDNA clone MGC:63319 IMAGE: ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=228805
www.ncbi.nlm.nih.gov
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Hutchinson-Gilford Progeria Syndrome
Atypical Werner syndrome [Chen et al 2003] ... GM, Mian IS, Kennedy BK, Oshima J. LMNA mutations in atypical Werner's syndrome. Lancet. ...
http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...
www.ncbi.nlm.nih.gov
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7327553 1982 04 12 1982 04 12 2007 11 14 0340-6717 58 3 1981 Hum. Genet ...
... Werner syndrome (adult progeria) was compared with the growth of ten FL cell ... Cocultivation of Werner syndrome and normal strains did not influence population ...
http://www.ncbi.nlm.nih.gov/pubmed/7327553?dopt=Abstract
www.ncbi.nlm.nih.gov
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Progeria: Causes - MayoClinic.com
Progeria ? Comprehensive overview covers causes, treatments of genetic disorder causing rapid ... Werner syndrome begins in adolescence or early adulthood. ...
http://www.mayoclinic.com/health/progeria/DS00936/DSECTION=causes
www.mayoclinic.com
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Orphanet: Werner syndrome
The portal for rare diseases and orphan drugs ... Werner syndrome. Orpha number. ORPHA902. Prevalence of ... Werner syndrome (WS) is a premature aging disease. ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=902
www.orpha.net
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Heart and circulation - Genetics Home Reference
Andersen cardiodysrhythmic periodic paralysis see Andersen-Tawil syndrome ... (AHD) see Alagille syndrome ... WS see Werner syndrome; Williams syndrome ...
http://ghr.nlm.nih.gov/conditionCategory=heartandcirculation
ghr.nlm.nih.gov
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Genes and Disease. Table of Contents
Genes and Disease provides an introduction to the relationship between genetic factors and human disease with a summary ... syndrome Werner syndrome Williams ...
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gnd.TOC&depth=2
www.ncbi.nlm.nih.gov
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Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg ...
Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, ... Werner syndrome (WS) is a progeroid syndrome caused by autosomal recessive null ...
http://www.ncbi.nlm.nih.gov/pubmed/11186893
www.ncbi.nlm.nih.gov
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Interaction of Werner and Bloom syndrome genes with p53 in familial ...
Interaction of Werner and Bloom syndrome genes with p53 in familial breast ... Werner Syndrome. Substances: Tumor Suppressor Protein p53. Exodeoxyribonucleases ...
http://www.ncbi.nlm.nih.gov/pubmed/16501249
www.ncbi.nlm.nih.gov
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Nucleolar localization of the Werner syndrome protein in human cells.
Werner Syndrome (WS) is a human genetic disorder with many features of premature ... Werner Syndrome/metabolism* Substances: Exodeoxyribonucleases. DNA ...
http://www.ncbi.nlm.nih.gov/pubmed/9618508
www.ncbi.nlm.nih.gov
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Laminopathy - Wikipedia, the free encyclopedia
Progeria with increased severity compared to normal Werner syndrome. Lamin A/C. 2003[12] ... LMNA mutations in atypical Werner's syndrome" ...
http://en.wikipedia.org/wiki/Laminopathy
en.wikipedia.org
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OMIM Update List for July, 1998
277700 WERNER SYNDROME; WRN. 312600 RETINITIS PIGMENTOSA 2; RP2 ... 277700 WERNER SYNDROME; WRN. 300075 RIBOSOMAL PROTEIN S6 KINASE, 90-KD, POLYPEPTIDE 3; RPS6KA3 ...
http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1998
www.ncbi.nlm.nih.gov
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Toxic Anterior Segment Syndrome After Cataract Surgery --- Maine, 2006
... HF, Dawson DG, Chew J, LeBoyer RM, Werner L. Toxic anterior segment syndrome. ... Werner L, Sher JH, Taylor JR, et al. Toxic anterior segment syndrome and ...
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5625a2.htm
www.cdc.gov
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A polymorphism in Werner syndrome gene is associated with breast cancer ...
RecQ helicases play a central role in maintaining genome stability and may ... genes WRN and BLM lead to rare autosomal recessive disorders, Werner and ...
http://www.ncbi.nlm.nih.gov/pubmed/19205873?dopt=Abstract
www.ncbi.nlm.nih.gov
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