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cockayne syndrome - rare genetic disorder with photosensitivity and neurological problems Definition for Cockayne Syndrome Cockayne syndrome (or "Weber-Cockayne syndrome", or "Neill-Dingwall Syndrome") is a rare, autosomal recessive disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. more Cockayne syndrome (or "Weber-Cockayne syndrome", or "Neill-Dingwall Syndrome") is a rare, autosomal recessive disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible. It is named after English physician Edward Alfred Cockayne (1880-1956). less some common symptoms delayed development face deformities rash scaly patches on skin some related diagnoses 1 - 3 of 3 diagnoses human immunodeficiency virus infections malnutrition drugs and toxins   more do i have 'Cockayne Syndrome'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'cockayne syndrome' 1 - 5 of 18 diagnostic tests BUN Cockayne Syndrome and BUN Complete metabolic panel Cockayne Syndrome and Complete metabolic panel EEG - Electroencephalogram Cockayne Syndrome and EEG - Electroencephalogram Hearing test standard technique of representing hearing loss Cockayne Syndrome and Hearing test Serum Creatinine Cockayne Syndrome and Serum Creatinine X-ray pelvis Cockayne Syndrome and X-ray pelvis X-ray spine Cockayne Syndrome and X-ray spine Brain MRI Cockayne Syndrome and Brain MRI CT brain Cockayne Syndrome and CT brain Electroretinogram (ERG) Cockayne Syndrome and Electroretinogram (ERG) Amniocentesis Cockayne Syndrome and Amniocentesis DNA mutation analysis Cockayne Syndrome and DNA mutation analysis Molecular Genetic Studies Cockayne Syndrome and Molecular Genetic Studies CT scan Cockayne Syndrome and CT scan Developmental testing Cockayne Syndrome and Developmental testing X-rays Cockayne Syndrome and X-rays serum electrolytes Cockayne Syndrome and serum electrolytes speech reception threshold (SRT) Cockayne Syndrome and speech reception threshold (SRT) for more please login, login is free (click to login) therapeutic procedures for 'Cockayne 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 Cockayne Syndrome: therapeutic procedure search results for 'cockayne syndrome' 1 - 4 of 4 therapeutic procedures rankings are computer generated. please consult your health care provider. Sun protection Cockayne Syndrome and Sun protection Physical and Occupational Therapy Arthritis Physical and Occupational Therapy Cockayne Syndrome and Physical and Occupational Therapy Special Education Cockayne Syndrome and Special Education Speech Therapy Cockayne Syndrome and Speech Therapy medications search results for 'cockayne syndrome' rankings are computer generated. please consult your health care provider. web search results for cockayne syndrome Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - Cockayne Syndrome Cockayne syndrome - Wikipedia, the free encyclopedia Xeroderma-pigmentosum-Cockayne syndrome (XP-CS) occurs when an individual also ... Mutations in the ERCC6 and ERCC8 genes are the cause of Cockayne syndrome. ... http://en.wikipedia.org/wiki/Cockayne_syndrome   en.wikipedia.org - summary Cockayne syndrome - Genetics Home Reference Cockayne syndrome can be divided into subtypes, which are distinguished by the ... Gene Review: Cockayne Syndrome. MedlinePlus Encyclopedia: Failure to Thrive ... http://ghr.nlm.nih.gov/condition=cockaynesyndrome   ghr.nlm.nih.gov - summary Cockayne syndrome Cockayne syndrome is a rare inherited disorder in which people are sensitive to ... onset or congenital form of Cockayne syndrome (Type II) is apparent at ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..Show...   www.ncbi.nlm.nih.gov - summary Cockayne Syndrome -- GeneReviews -- NCBI Bookshelf Cockayne syndrome (referred to as CS throughout this GeneReview) spans a ... Cockayne syndrome is inherited in an autosomal recessive manner. ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=cockayne   www.ncbi.nlm.nih.gov - summary Cockayne syndrome - References - Genetics Home Reference The bases for Cockayne syndrome. Nature. 2000 May 25;405(6785):415-6. No abstract available. ... among 13 new Cockayne syndrome cases confirmed by biochemical ... http://ghr.nlm.nih.gov/condition=cockaynesyndrome/show/References   ghr.nlm.nih.gov - summary Cockayne Syndrome Cockayne syndrome (referred to as CS throughout this ... pigmentosum-Cockayne syndrome (XP-CS) includes facial freckling and early skin cancers ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Response of motor complications in Cockayne syndrome to carbidopa-levodopa. ... difficulties are common features of Cockayne syndrome that are consequences ... CONCLUSIONS: Patients with Cockayne syndrome should be evaluated carefully for ... http://www.ncbi.nlm.nih.gov/pubmed/18695064?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary Cockayne syndrome - Patient support - For patients and families ... Genetic Conditions > Cockayne syndrome > Patient support - For patients and families ... in the Genetics Home Reference condition summary on Cockayne syndrome. ... http://ghr.nlm.nih.gov/condition=cockaynesyndrome/show/Patient+support   ghr.nlm.nih.gov - summary Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and ... Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes. ... abnormality seen in Cockayne syndrome (CS), one of the ... http://www.ncbi.nlm.nih.gov/pubmed/1372469   www.ncbi.nlm.nih.gov - summary Infantile onset of Cockayne syndrome in two siblings. Infantile onset of Cockayne syndrome in two siblings. Batra P, Saha A, Kumar A. ... Cockayne Syndrome/genetics* Cockayne Syndrome/pathology* Family Health ... http://www.ncbi.nlm.nih.gov/pubmed/18187833?ordinalpos=95&it...   www.ncbi.nlm.nih.gov - summary Characterisation of novel mutations in Cockayne syndrome type A and ... We report that a subject with Cockayne syndrome type A (CS3BE) was a compound ... Cockayne Syndrome/genetics* DNA Primers. DNA Repair Enzymes. DNA-Binding ... http://www.ncbi.nlm.nih.gov/pubmed/15744458   www.ncbi.nlm.nih.gov - summary Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: do ... Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy are three ... Cockayne Syndrome/genetics* DNA Repair. Genes, Overlapping. Hair Diseases ... http://www.ncbi.nlm.nih.gov/pubmed/8984734   www.ncbi.nlm.nih.gov - summary Cockayne syndrome group B protein enhances elongation by RNA polymerase II. Cockayne syndrome group B protein enhances elongation by RNA ... Cockayne syndrome (CS) is characterized by impaired physical and mental development. ... http://www.ncbi.nlm.nih.gov/pubmed/9326587   www.ncbi.nlm.nih.gov - summary Cockayne Syndrome - Yahoo! Health Important It is possible that the main title of the report Cockayne Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ... http://health.yahoo.com/children-genetic/cockayne-syndrome/h...   health.yahoo.com - summary COCKAYNE SYNDROME - Pedbase.org PEDBASE.org - The Pediatric Database - Detailed information of COCKAYNE SYNDROME ... 1994 -2007 Pedbase.org. Powered by Database of Pediatrics- COCKAYNE SYNDROME ... http://www.pedbase.org/c/cockayne-syndrome   www.pedbase.org - summary Clinical implications of the basic defects in Cockayne syndrome and ... ... of the basic defects in Cockayne syndrome and xeroderma pigmentosum and the DNA ... Cockayne Syndrome/diagnosis. Cockayne Syndrome/drug therapy. Cockayne ... http://www.ncbi.nlm.nih.gov/pubmed/18336867?ordinalpos=6&ito...   www.ncbi.nlm.nih.gov - summary Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome ... Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A. ... These kinetics resembled those of Cockayne syndrome (CS) cells. ... http://www.ncbi.nlm.nih.gov/pubmed/8596535   www.ncbi.nlm.nih.gov - summary Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B ... Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells. ... in DNA by normal and Cockayne Syndrome (CS) cell extracts has been investigated. ... http://www.ncbi.nlm.nih.gov/pubmed/9973627   www.ncbi.nlm.nih.gov - summary Epidermolysis bullosa ... bullosa; Hemidesmosomal epidermolysis bullosa; Weber-Cockayne syndrome ... For example, Weber-Cockayne is the most common form of epidermolysis bullosa simplex. ... http://adam.about.com/encyclopedia/infectiousdiseases/Epidermolysis-bullosa.htm   adam.about.com - summary Bones, muscles, and connective tissues - Genetics Home Reference Cockayne-Pelizaeus-Merzbacher Disease see Pelizaeus-Merzbacher disease. Cockayne syndrome ... CS see Cockayne syndrome. CUD see primary carnitine deficiency ... http://www.ghr.nlm.nih.gov/conditionCategory=bonesmusclesandconnectivetissues   www.ghr.nlm.nih.gov - summary Edward Alfred Cockayne - Wikipedia, the free encyclopedia Cockayne syndrome III: milder than Cockayne I & II, and its onset happens later ... Additional information on Cockayne's Syndrome (PDF) Who Named It?; Edward Cockayne ... http://en.wikipedia.org/wiki/Edward_Alfred_Cockayne   en.wikipedia.org - summary Health Library - Avera Health Waterhouse-Friderichsen syndrome. Wax blockage. Weak bones - premature infants. Weber-Cockayne syndrome. Wegener's granulomatosis. Weil disease. Welts. Werdnig ... http://averaorg.adam.com/content.aspx?productId=101&alpha=W&sub=Disease   averaorg.adam.com - summary Progeria: Miscellaneous Disorders in Infants and Children: Merck Manual ... Progeria is a rare syndrome of accelerated aging that manifests early in ... 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 - summary CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new ... CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism. ... found that a subject with Cockayne syndrome type A was a compound ... http://www.ncbi.nlm.nih.gov/pubmed/14661080   www.ncbi.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Hearing loss Leopard syndrome (multiple lentigines) Otosclerosis. Robinson type ... Cockayne syndrome. Bjorn pili torti and deafness syndrome. Multiple synostosis syndrome ... http://www.nlm.nih.gov/medlineplus/ency/article/003044.htm   www.nlm.nih.gov - summary 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 health ... Cochlear Implants. Cockayne Syndrome ... http://www.webmd.com/a-to-z-guides/health-topics/ck-co.htm   www.webmd.com - summary CAMFAK syndrome - Wikipedia, the free encyclopedia ... of nerves, similar to that seen in Cockayne syndrome.[1] ... CAMFAK syndrome: a demyelinating inherited disease similar to Cockayne syndrome". Am. ... http://en.wikipedia.org/wiki/CAMFAK_syndrome   en.wikipedia.org - summary Li-Fraumeni syndrome - Wikipedia, the free encyclopedia Li-Fraumeni Syndrome by Katherine A Schneider and Frederick Li, in GeneReviews, ... syndrome · Cockayne syndrome · Fanconi anemia · Li-Fraumeni syndrome ... http://en.wikipedia.org/wiki/Li-Fraumeni_syndrome   en.wikipedia.org - summary Chromosome 10 - Conditions related to genes on chromosome 10 - Genetics ... Apert syndrome. autosomal dominant partial epilepsy with auditory features ... Cockayne syndrome. Cornelia de Lange syndrome. Cowden syndrome. Crouzon syndrome ... http://ghr.nlm.nih.gov/chromosome=10/show/Conditions   ghr.nlm.nih.gov - summary ERCC6 - excision repair cross-complementing rodent repair deficiency ... Cockayne syndrome - caused by mutations in the ERCC6 gene. More than 20 ERCC6 mutations that cause Cockayne syndrome have been identified. ... http://ghr.nlm.nih.gov/gene=ercc6   ghr.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Epidermolysis bullosa ... bullosa; Hemidesmosomal epidermolysis bullosa; Weber-Cockayne syndrome ... For example, Weber-Cockayne is the most common form of epidermolysis bullosa simplex. ... http://www.nlm.nih.gov/medlineplus/ency/article/001457.htm   www.nlm.nih.gov - summary Role of the ATPase domain of the Cockayne syndrome group B protein in ... ... the ATPase domain of the Cockayne syndrome group B protein in UV ... Cockayne syndrome (CS) is a human autosomal recessive disorder characterized by ... http://www.ncbi.nlm.nih.gov/pubmed/10698517?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Werner syndrome - Wikipedia, the free encyclopedia Cockayne syndrome. DNA repair. Degenerative disease. Genetic disorder. Life extension ... syndrome · Cockayne syndrome · Fanconi anemia · Li-Fraumeni syndrome ... http://en.wikipedia.org/wiki/Werner_syndrome   en.wikipedia.org - summary ERCC8 - excision repair cross-complementing rodent repair deficiency ... Cockayne syndrome - caused by mutations in the ERCC8 gene. Researchers have identified several ERCC8 mutations that cause Cockayne syndrome. ... http://ghr.nlm.nih.gov/gene=ercc8   ghr.nlm.nih.gov - summary Site Map od Pedbase.org - The Pediatric Database Pedbase Site Map. Pediatric. Site Map. Resources. Contact. PEDBASE.org - The Pediatric Database. A. B. C. D. E. F. G. H. I. J. K. L. M. N. O. P. R. S. T. U. V. W. X ... http://pedbase.org/sitemap.html   pedbase.org - summary Disease Reference Waterhouse-Friderichsen syndrome. Wax blockage. Weak bones - premature infants. Weber-Cockayne syndrome. Wegeners granulomatosis. Weil disease. Welts. Werdnig ... http://adam.about.com/HIE/diseidxw.htm   adam.about.com - summary : Mercy Adam Content : Weber-Cockayne syndrome. Weedoff poisoning. Weedy nightshade poisoning. Wegener's granulomatosis ... Wolff-Parkinson-White syndrome. Women and heart disease ... http://mercycanton3.adam.com/content.aspx?productId=101&alpha=W   mercycanton3.adam.com - summary Zori Stalker Williams syndrome - Wikipedia, the free encyclopedia Zori Stalker Williams syndrome at NIH's Office of Rare Diseases ... syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome ... http://en.wikipedia.org/wiki/Zori_Stalker_Williams_syndrome   en.wikipedia.org - summary A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome ... ... gene, associated with xeroderma pigmentosum B (XP-B) and Cockayne's syndrome (CS) ... Cockayne Syndrome/genetics* DNA Repair/genetics. DNA-Binding Proteins ... http://www.ncbi.nlm.nih.gov/pubmed/1458540   www.ncbi.nlm.nih.gov - summary Hearing loss Bjorn pili torti and deafness syndrome. Cockayne syndrome. Fronto-metaphyseal dysplasia syndrome ... Waardenburg syndrome. Congenital: Congenital atresia of ... http://adam.about.com/encyclopedia/Hearing-loss.htm   adam.about.com - summary MedlinePlus Medical Encyclopedia: Topics beginning with W Weber-Cockayne syndrome see Epidermolysis bullosa ... Wermer syndrome see Multiple endocrine neoplasia (MEN) I ... WPW see Wolff-Parkinson-White syndrome. Wrinkles ... http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_W.htm   www.nlm.nih.gov - summary The ATPase domain but not the acidic region of Cockayne syndrome group ... Cockayne syndrome (CS) is a human genetic disorder characterized by UV ... Cockayne Syndrome/genetics. Cricetinae. DNA Damage. DNA Helicases/chemistry. DNA ... http://www.ncbi.nlm.nih.gov/pubmed/10564257?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Cockayne syndrome - Educational resources - Information pages ... Genetic Conditions > Cockayne syndrome > Educational resources - Information pages ... in the Genetics Home Reference condition summary on Cockayne syndrome. ... http://ghr.nlm.nih.gov/condition=cockaynesyndrome/show/Educational+resources   ghr.nlm.nih.gov - summary Fountain syndrome - Wikipedia, the free encyclopedia Fountain syndrome is an autosomal recessive congenital disorder characterized by ... syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome ... http://en.wikipedia.org/wiki/Fountain_syndrome   en.wikipedia.org - summary Keutel syndrome - Wikipedia, the free encyclopedia Keutel syndrome is a rare autosomal recessive genetic disorder characterized by ... syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome ... http://en.wikipedia.org/wiki/Keutel_syndrome   en.wikipedia.org - summary Dwarfism - Genetics Home Reference Cockayne syndrome. congenital hypothyroidism. diastrophic dysplasia. Ellis-van Creveld syndrome ... Melnick-Needles syndrome. platyspondylic lethal skeletal ... http://ghr.nlm.nih.gov/conditionGroup=dwarfism   ghr.nlm.nih.gov - summary Genes and Disease. Table of Contents Genes and Disease provides an introduction to the relationship between genetic factors and human disease with a summary of ... cancer Cockayne syndrome Diabetes, ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gnd.TOC&depth=2   www.ncbi.nlm.nih.gov - summary Encyclopedia C-Cz on Yahoo! Health Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, ... Cockayne Syndrome. Codependency ... http://health.yahoo.com/ency/c/   health.yahoo.com - summary Branchio-oto-renal syndrome - Wikipedia, the free encyclopedia Branchiootorenal syndrome from Gene Reviews. v ? d ? e ... syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome ... http://en.wikipedia.org/wiki/Branchio-oto-renal_syndrome   en.wikipedia.org - summary Search Results - Genetics Home Reference Found: ...syndrome is a common form of syndromic deafness (hearing loss that ... Cockayne syndrome. Condition summary ... with CHARGE syndrome also typically... http://ghr.nlm.nih.gov/search?query=hearing+loss&show=conditions   ghr.nlm.nih.gov - summary show more 1  2