41. Incontinentia Pigmenti Translate this page Cette page utilise des cadres, mais votrenavigateur ne les prend pas en charge. http://www.atlas-dermato.org/atlas/incontinentiafin.htm

Cette page utilise des cadres, mais votre navigateur ne les prend pas en charge.

42. Incontinentia Pigmenti Translate this page incontinentia pigmenti. Syndrome héréditaire complexe qui atteintpresque exclusivement des filles. Signes cutanés une phase http://www.atlas-dermato.org/atlas/incontinentiaico.htm

Incontinentia Pigmenti Syndrome héréditaire complexe qui atteint presque exclusivement des filles. Signes cutanés : une phase bulleuse initiale néonatale ; plaques érythémato-papuleuses recouverte de bulles, une phase papulokératosique (2-5mois) ; des papules d'allure lichénoïdes secondairement recouvertes d'épaisses verrucosités papillomateuses sur les zones bulleuses, souvent à disposition linéaire, phase pigmentée (3-6 mois) ; macules ardoisées distribuée en éclaboussures, en jet d'eau, sur le thorax et les membres. Biopsie d'une papule kératosique Retour Atlas

43. OM INCONTINENTIA PIGMENTI OM incontinentia pigmenti. http://medlem.jubii.dk/ipd/omip.htm

OM INCONTINENTIA PIGMENTI Forside Baggrund Kilder og Links Bliv medlem Hvad er IP IP er en genetisk sygdom (der sidder på X-kromosomet) der ses på hud, hår, tænder, øjne og det centrale nervesystem. Sygdommen fik sit navn pga. hudens udseende under mikroskop. Det blev først beskrevet i 1906 af Garrod, men den første komplette beskrivelse blev skrevet af Bloch og Sulzberger i 1928 - deraf navnet Bloch-Sulzberger syndrom som sygdommen også kaldes. Al genetisk information er arvet fra vore forældre. Som de fleste ved er X-kromosomet livsvigtigt - begge køn har det. Hunkøn har 2 X-kromosomer mens hankøn har 1 X-kromosom og 1 Y-kromosom. Derfor er der nogle sygdomme, der kun rammer hunkøn hvor hankøn automatisk vil dø, pga. antallet af X-kromosomer som er tilfældet ved IP. Dvs. at det er kun hunkøn der overlever sygdommen. Det betyder at hunkøn har et defekt gen, forårsaget af en mutation, på det ene X-kromosom og et ganske normalt X-kromosom. IP vil altid være at se, men man kan ikke sige hvor udtalt den vil være hos hvert enkelt individ. En kvinde der har IP vil ved enhver graviditet give halvdelen af hendes genetiske informationer til fosteret. Der vil være 50% chance for at videreføre X-kromosomet med det defekte gen uanset fosterets køn.

44. X-linked Dominant: Incontinentia Pigmenti - Lucile Packard Children's Hospital Xlinked Dominant incontinentia pigmenti Genes are inherited from our biologicalparents in specific ways. What is incontinentia pigmenti (IP)? http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/genetics/xdomin.html

Genetics Clinic Metabolic/Biochemical Genetics Clinic Medical Geneticists Medical Genetics Medical Genetics X-linked Dominant: Incontinentia Pigmenti Genes are inherited from our biological parents in specific ways. One of the basic patterns of inheritance of our genes is called X-linked dominant inheritance. What is X-linked dominant inheritance? X-linked dominant inheritance is where the gene is located on the X chromosome, but the gene acts in a dominant manner. This means that both males and females can display the trait or disorder, by only having one copy of the gene. Depending on the disorder, often times a gene that is X-linked dominant causes a male pregnancy not to survive. Another way scientists and physicians refer to this process is to say that "there is lethality in males." This means that the gene is passed from mother to daughter, and, if passed to a son, the pregnancy miscarries. Only those sons without the gene survive to be born and are born healthy. One example of an X-linked dominant condition is called incontinentia pigmenti (IP). What is incontinentia pigmenti (IP)?

45. Incontinentia Pigmenti incontinentia pigmenti. incontinentia pigmenti (IP) (BlochSulzbergersyndrome) is an X-linked dominant disorder seen in females http://www.kidseyecancer.org/pro/cme/cme_28.htm

RBI Home What Is Retinoblastoma? ... Us Page Not Found Our site has recently changed. Please select from the choices above. Graphic Design by Ad One Hosting and Web Design by Wakai

46. Health Library - Incontinentia Pigmenti incontinentia pigmenti. incontinentia pigmenti (IP) is a rare genetic dermatologicaldisorder affecting the skin, hair, teeth, and central nervous system. http://www.laurushealth.com/Library/HealthGuide/IllnessConditions/topic.asp?hwid

47. Health Library - Incontinentia Pigmenti incontinentia pigmenti. Self Help Clearinghouse. National IncontinentiaPigmenti Foundation. National network. Founded http://www.laurushealth.com/library/healthguide/selfhelp/topic.asp?hwid=shc29inp

48. Health Library - Incontinentia Pigmenti incontinentia pigmenti. Self Help Clearinghouse. National IncontinentiaPigmenti Foundation. National network. Founded http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29i

49. Health Library - Incontinentia Pigmenti Saint Luke's Health System eLibrary. incontinentia pigmenti. Self Help Clearinghouse.National incontinentia pigmenti Foundation. National network. http://hvelink.saint-lukes.org/library/healthguide/SelfHelp/topic.asp?hwid=shc29

50. Health Information Resource Database: Incontinentia Pigmenti International Found incontinentia pigmenti International Foundation, Inc. Contact Information. Abstract.Founded in 1995, the incontinentia pigmenti International Foundation, Inc. http://www.health.gov/nhic/NHICScripts/Entry.cfm?HRCode=HR3105

51. Online Dermatology Image Library Next Result Set. THIGH incontinentia pigmenti © 200102, Johns Hopkins UniversitySchool of Medicine Dermatlas, Image Name ip_1_020627, File Type jpg. http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=166

52. Incontinentia Pigmenti Translate this page Prof. Dr. JG Casas. incontinentia pigmenti. incontinentia pigmenti. Incontinentiapigmenti. Arriba Queratosis seborreica. Hidroacantoma simplex. http://www.seap.es/reuniones/almagro2000/casas/nidosg2.htm

Curso Internacional de Dermatopatología Arriba Queratosis seborreica. Hidroacantoma simplex. Enfermedad de Bowen [ Incontinentia pigmenti ] Nevo recurrente - Melanoma Células de Langerhans - Micosis fungoide Enfermedad de Paget - Carcinoma apocrino Papulosis de células claras ... Carcinoma de células de Merkel Nidos intraepidérmicos Prof. Dr. J. G. Casas Incontinentia pigmenti Incontinentia pigmenti Incontinentia pigmenti Arriba Queratosis seborreica. Hidroacantoma simplex. Enfermedad de Bowen [ Incontinentia pigmenti ] Nevo recurrente - Melanoma Células de Langerhans - Micosis fungoide Enfermedad de Paget - Carcinoma apocrino Papulosis de células claras ... Carcinoma de células de Merkel

53. GeneReviews: Incontinentia Pigmenti Your browser does not support HTML frames so you must view incontinentia pigmentiin a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/i-p/

Your browser does not support HTML frames so you must view Incontinentia Pigmenti in a slightly less readable form. Please follow this link to do so.

54. Incontinentia Pigmenti International Foundation Return to Search Page incontinentia pigmenti International Foundation. EmailIPIF@IPIF.org. Conditions incontinentia pigmenti. Hours Answered 9am - 5pm http://www.geneticalliance.org/Resources/displayorganization.html?orgname=Incont

55. Incontinentia Pigmenti International Foundation incontinentia pigmenti International Foundation. 30 E 72nd St New York,NY 10021 Conditions incontinentia pigmenti. Hours Answered MF, 105 http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Inco

56. 1Up Health > Incontinentia Pigmenti Achromians > Causes, Incidence, And Risk Fac Comprehesive information on incontinentia pigmenti achromians (Hypomelanosis ofIto). incontinentia pigmenti achromians Causes, Incidence, and Risk Factors. http://www.1uphealth.com/health/incontinentia_pigmenti_achromians_info.html

1Up Health Incontinentia pigmenti achromians Alternative Medicine Clinical Trials ... Health Topics A-Z Search 1Up Health Incontinentia pigmenti achromians Information Incontinentia pigmenti achromians Causes, Incidence, and Risk Factors Alternative names : Hypomelanosis of Ito Definition : A congenital disorder that causes unusual and sometimes bizarre patterns of hypopigmented (diminished pigment) skin. Causes, Incidence, and Risk Factors The cause of this disorder is unknown, though most patients have abnormal chromosomes. Girls are affected slightly more often than boys. Previous Next Jump to Another Section of this Guide Definition Causes, Incidence, and Risk Factors Symptoms Diagnosis, Signs, and Tests Treatment Prognosis (Expectations) ... Calling your Health Care Provider Related Tools and Utilities Search Books on Amazon: Read Articles on eLibrary: Health Products on drugstore.com: Review Date Reviewed By : Michael Lehrer, M.D., Department of Dermatology, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network. Guide Definition Causes, Incidence, and Risk Factors

57. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders Sites. Drkoop.com Medical Encyclopedia Information about incontinentia pigmenti,its causes, symptoms, tests, diagnosis, treatment and possible complications. http://www.1uphealth.com/links/genetic-disorders-incontinentia-pigmenti.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Genetic Disorders : Incontinentia Pigmenti Description Sites Drkoop.com: Medical Encyclopedia Information about incontinentia pigmenti, its causes, symptoms, tests, diagnosis, treatment and possible complications. Incontinentia Pigmenti Informational sheet compiled by National Institute of Neurological Disorders and Stroke. Incontinentia Pigmenti: All About Anna The authors' daughter was diagnosed with IP 6 weeks after birth. This is her story. Incontinentia Pigmenti International Foundation Details about the organization that is dedicated to research into the causes and treatment of this genetic disease. Includes information about the disease, genetics and genes. MCW Healthlink: Incontinentia Pigmenti An article about this rare genetic disorder, its stages and symptoms. National Library of Medicine Bloch-sulzberger syndrome, the synonyms, a summary and major features.

58. A Skinpatient's World - Incontinentia Pigmenti incontinentia pigmenti ( IP ). Other names – Bloch Schulzberger syndrome.Bloch Siemens syndrome. IP is a distinctive syndrome transmitted http://www.skinpatient.com/ptinfo/I/incontinentiapigmenti.htm

59. Incontinentia Pigmenti incontinentia pigmenti. What is incontinentia pigmenti? Incontinentiapigmenti (IP) is a rare, genetic disorder characterized by http://www.clevelandclinic.org/health/health-info/docs/1200/1290.asp?index=6042

60. Retina International's Scientific Newsletter - Incontinentia Pigmenti Loci Scientific Newsletter. Disease Database incontinentia pigmenti. Recent updatefrom 08.02.2001 incontinentia pigmenti type 2, IP2, 308310, xl, Xq28. http://www.retina-international.org/sci-news/incopig.htm

Retina International's Scientific Newsletter Disease Database Incontinentia Pigmenti Recent update from: 08.02.2001 Disease Gene locus MIM Gene Gene MIM MoI Assignment Linked Marker [cM] Remarks References Bloch-Sulzberger syndrome xl Hypomelanosis of Ito ar 9q33-ter, Xp11, 15q11-13 Incontinentia pigmenti type 2 xl cen- DXS1296-IDS- DXS455- DXS304- DXS374- DXS52- DXS33- DXS134- DXS15- CV(RCP/GCP)-G6PD-F8C- DXS115- DXS108- DXYS154 MoI = Mode of Inheritance: a: autosomal, ad: autosomal dominant, ar: autosomal recessive, xl: x-linked, mt: mitochondrial References . Happle,R. Tentative assignment of hypomelanosis of Ito to 9q33qter. 1987; Hum.Genet. 75: 98-99. Link to PudMed Goto Top . Koiffmann,C.P., de Souza,D.H., Diament,A., Ventura,H.B., Alves,R.S., Kihara,S., and Wajntal,A. Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11. 1993; Am.J.Med.Genet. 46: 529-533. Link to PudMed Goto Top . McDonald,M., Bialecki,M., Van Antwerp,M., Burright,E., Trask,B., and Gorsky,J. A 1.2 Mb YAC contig maps two incontinentia pigmenti type I (IP1) disease translocation breakpoints map to an 80 kb interval. 1995; Am.J.Hum.Genet. 57: A264 Goto Top . Pellegrino,J.E., Schnur,R.E., Kline,R., Zackai,E.H., and Spinner,N.B. Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? 1995; Hum.Genet. 96: 485-489.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 3     41-60 of 95    Back | 1  | 2  | 3  | 4  | 5  | Next 20