61. 1927 Neonatal Incontinentia Pigmenti In An Affected Male Within Neonatal incontinentia pigmenti in an affected male within a normal family. IncontinentiaPigmenti (IP) is a rare Xlinked dominant genodermatosis. http://www.faseb.org/genetics/ashg99/f1927.htm

62. 2095 Skewed X-inactivation In Incontinentia Pigmenti (IP2). Program Nr 2095 Skewed Xinactivation in incontinentia pigmenti (IP2). A.Smahi, S. Heuertz, JP Bonnefont, A. Delanay, P. Vabres, A. Munnich. http://www.faseb.org/genetics/ashg99/f2095.htm

63. Medical Genetics - X-linked Dominant: Incontinentia Pigmenti Xlinked Dominant incontinentia pigmenti Genes One example of an X-linkeddominant condition is called incontinentia pigmenti (IP). What http://www.chkd.org/Genetics/xdomin.asp

More Health Information Adolescent Medicine Allergy/Immunology Anesthesiology Arthritis Burns Cardiology Craniofacial Dental Medicine Dermatology Developmental Peds Diabetes Digestive Ear, Nose, Throat Genetics Gastroenterology Growth Hematology High Risk Newborn High Risk Pregnancy Infectious Disease Mental Health Neonatology Nephrology Neurology Normal Newborn Normal Pregnancy Oncology Ophthalmalogy Orthopaedics Otolaryngology Pediatric Intensive Care Pediatric Surgery Pediatrics Physical Medicine Plastic Surgery Respiratory/Pulmonology Rheumatology Safety Surgery Terminal Transplant Urology Site Search For a doctor who specializes in this topic, click here. 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).

64. Incontinentia Pigmenti - HUM-MOLGEN Author, Topic incontinentia pigmenti. I have a patient with incontinentia pigmenti.She is 4 months old, there isn't any other patient in her family. http://www.hum-molgen.de/bb/Forum2/HTML/000073.html

home genetic news bioinformatics biotechnology ... DIAGnostics - Clinical Research (professional requests) Incontinentia Pigmenti profile register preferences faq ... next oldest topic Author Topic: Incontinentia Pigmenti Fatma SILAN Member posted 04-17-2001 09:52 AM Dear Colleagues, I am geneticist at Duzce Medical Faculty-Turkey. I have a patient with Incontinentia Pigmenti. She is 4 months old, there isn't any other patient in her family. If you interest IP or Xq11(?), I can send you her blood samples. Thanks for collaboration Yr.Doc.Dr. Fatma SILAN AIBU Duzce Medical Faculty Medical Biology and Genetics, Chair IP: 193.140.158.120 All times are ET (US) next newest topic next oldest topic Administrative Options: Close Topic Archive/Move Delete Topic Hop to: Select a Forum or Archive List of Forums: Biotechnical requests and sources DIAGnostics - Clinical Research (professional requests) Ethical, legal and social implications Open Topic Forum List of Archives: Genetic News Contact Us HUM-MOLGEN HUM-MOLGEN Powered by: Ultimate Bulletin Board, Version 5.44a By posting requests at HUM-MOLGEN you reach more than 8.000 mailing list subscribers and a 6 digit number of www users. Therefore post high quality messages only, including full name and institutional address.

65. Preimplantation Diagnosis For IP (Incontinentia Pigmenti) - HUM-MOLGEN Author, Topic Preimplantation diagnosis for IP (incontinentia pigmenti). Weare caring for a family with IP (incontinentia pigmenti). http://www.hum-molgen.de/bb/Forum2/HTML/000047.html

home genetic news bioinformatics biotechnology ... DIAGnostics - Clinical Research (professional requests) Preimplantation diagnosis for IP (Incontinentia pigmenti) profile register preferences faq ... next oldest topic Author Topic: Preimplantation diagnosis for IP (Incontinentia pigmenti) Administrator Administrator posted 09-11-2000 09:53 AM We are caring for a family with IP (Incontinentia pigmenti). Two affected sisters apparently have the common insertion mutation. The family is seeking pre-implantation diagnosis. Moshe Frydman MD Associate Professor of Pediatrics and Medical Genetics, The Danek Gertner Institute of Human Genetics Chaim Sheba Medical Center, Tel Hashomer, 52621, Israel E-mail: mfrydman@POST.TAU.AC.IL IP: 160.45.191.21 Administrator Administrator posted 04-17-2001 01:50 PM Genetic diagnosis for IP is available through the Baylor DNA Diagnostic Laboratory at www.bcmgeneticlab.org Richard Alan Lewis M.D., M.S. Professor, Departments of Ophthalmology, Medicine, Voice: 713-798-3030; Fax: 713-798-3042 IP: 160.45.191.21 All times are ET (US) next newest topic next oldest topic Administrative Options: Close Topic Archive/Move Delete Topic Hop to: Select a Forum or Archive List of Forums: Biotechnical requests and sources DIAGnostics - Clinical Research (professional requests) Ethical, legal and social implications

66. Incontinentia Pigmenti Kehitysvammahuollon tietopankki. incontinentia pigmenti, tyyppi II BlochSulzbergerinoireyhtymä. incontinentia pigmenti (IP). Incontinentia http://www.saunalahti.fi/kup/syndroma/ip.htm

Kehitysvammahuollon tietopankki Incontinentia Pigmenti, tyyppi II Bloch-Sulzbergerin oireyhtymä Incontinentia Pigmenti (IP) Incontinentia Pigmenti (IP) on harvinainen vallitsevasti periytyvä sairaus. Sen aiheuttaa X-krosomin geeni, mahdollisesti kaksikin. Geenikartoissa mainitaan alueet Xp11.21 ja Xq28. IP-tauti aiheuttaa iho-oireita, minkä lisäksi siihen liittyy silmien, keskushermoston ja hampaiston vaurioita. Myös kynsien ja hiusten vaillinaisuuksia esiintyy usein. Niinikään pienipäisyydestä mainitaan sairautta koskevissa raporteissa. Iho-oireet ilmenevät vaiheittain. Vastasyneen iho on punanainen ja rakkuloiva. Seuraavalla tasolla esiintyy käsien ja jalkapohjien rupia. Kolmannessa vaiheessa muodostuu ylipigmentoituneita ihoalueita, ja lopuksi ihon kalvakoitumista, kuivumista ja arpeutumista. Keskushermostovauriot ilmenevät epilepsiana tetraplegiana ja kehitysvammaisuutenakin IP-tauti on yleisempi naisilla kuin miehillä. Sen esiintyvyydestä ei ole tarkkoja tietoja. Lievästi vammautuneiden arvellaan jäävän usein huomaamatta. Lisätietoja: Maarit Peippo: Incontinentia pigmenti (IP) , Väestöliitto, Perinnöllisyysklinikan tietolehtiset

67. Medical Genetics - X-linked Dominant: Incontinentia Pigmenti Xlinked Dominant incontinentia pigmenti. Genes are inherited from our biologicalparents in specific ways. What is incontinentia pigmenti (IP)? http://www.musckids.com/health_library/genetics/xdomin.htm

Home About Us Departments MUSC eNurse ... Your Hospital Visit 171 Ashley Ave. Charleston, SC 29425 800-424-MUSC Print Version 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)?

68. Incontinentia Pigmenti Achromians incontinentia pigmenti achromians. Definition A congenital disorderthat causes unusual and sometimes bizarre patterns of hypopigmented http://www.pennhealth.com/ency/article/001461.htm

Disease Injury Nutrition Poison ... Prevention Incontinentia pigmenti achromians Definition: A congenital disorder that causes unusual and sometimes bizarre patterns of hypopigmented (diminished pigment) skin. Alternative Names: Hypomelanosis of Ito 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. Review Date: 12/2/2001 Reviewed By: Michael Lehrer, M.D., Department of Dermatology, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

69. Incontinentia Pigmenti On The Leg back. incontinentia pigmenti produces darklypigmented swirling markson the skin. It occurs more frequently in females. The skin http://www.pennhealth.com/imagepages/2861.htm

Incontinentia pigmenti produces darkly-pigmented swirling marks on the skin. It occurs more frequently in females. The skin lesions are divided into three stages: blisters (vesicles and bullae) are present at birth or within the first 6 to 7 weeks, followed by a rough wart-like (verrucous) stage, and lastly, swirled and bizarre patterns of dark pigmentation (hyperpigmentation) appear. Acquired Date: 1/1/1997 12:00:00 AM Acquired From: Mosby Publishing Company

70. Alopecia Relating To Incontinentia Pigmenti Alopecia relating to incontinentia pigmenti. Comments. My daughter was born with agenetic disorder incontinentia pigmenti . One of the conditions is alopecia. http://members.tripod.com/alopecia/_disc3/00000008.htm

71. Incontinentia Pigmenti - Wikipedia NL incontinentia pigmenti. incontinentia pigmenti (Ook syndroom van BlochSulzbergerof syndroom van Bloch-Siemens genaamd) is een zeldzame (ca. http://nl.wikipedia.org/wiki/Incontinentia_pigmenti

Hoofdpagina Recente wijzigingen Pagina bewerken Voorgeschiedenis Speciale pagina's Mijn gebruikersvoorkeuren instellen Mijn volglijst tonen Recent bijgewerkte pagina's tonen Afbeeldingen uploaden Lijst ge-uploade afbeeldingen tonen Geregistreerde gebruikers tonen Statistieken tonen Ga naar een willekeurig artikel Niet-gelinkte artikels tonen Niet-gelinkte afbeeldingen tonen Populaire artikels tonen Meest gewenste artikels tonen Korte artikels tonen Lange artikels tonen Nieuwe artikels tonen Taallinks Alle paginatitels tonen Geblokkeerde IP-adressen tonen Onderhoudspagina Boekhandels Printer-vriendelijke versie Overleg Aanmelden Help Incontinentia pigmenti Incontinentia pigmenti (Ook syndroom van Bloch-Sulzberger of syndroom van Bloch-Siemens genaamd) is een zeldzame (ca. 1:30.000) erfelijke (x-gebonden dominante ) huidziekte die wordt gekenmerkt door onregelmatige pigmentatie van de huid, met name bij jonge kinderen. De huidmanifestaties verdwijnen vaak zonder behandeling in de adolescentie. Naast huidafwijkingen kunnen er ook neurologische en oogsymptomen en tand- en skeletafwijkingen bij voorkomen. De ziekte komt meestal bij vrouwen/meisjes voor omdat aangedane mannelijke vruchten meestal al voor de geboorte doodgaan. De plaats van de genetische afwijking is sinds 1999 bekend en ligt op de locatie Xq28 in het zgn. NEMO gen. externe links http://www.ninds.nih.gov/health_and_medical/disorders/inconpig_doc.htm

72. Incontinentia Pigmenti incontinentia pigmenti. Image URL Erythema dyschromicum perstans, ImageURL Lichen planus vesicular lesion, Image URL Pigmentary incontinence, http://www.brisbio.ac.uk/ROADS/subject-listing/incontinentiapigmenti.html

A collection of medical, dental and veterinary images for use in teaching. Home About the Archive FAQ Terms and Conditions ... Help Incontinentia Pigmenti Erythema dyschromicum perstans Lichen planus vesicular lesion Pigmentary incontinence Pigmentary incontinence in lichen planus Pigmentary incontinence in lichen planus Pigmentary incontinence Pigmentary incontinence

73. Incontinentia Pigmenti Subscribe now . incontinentia pigmenti. incontinentia pigmenti (IP) is a rare,genetic disorder characterized by unusual patterns of discolored skin. http://oci.mcw.edu/article/921770674.html

Search: search tips Email this article Print this article Find related articles: By topic: Neurology By keywords: Receive Health Link via email! Subscribe now >> Incontinentia Pigmenti Incontinentia pigmenti (IP) is a rare, genetic disorder characterized by unusual patterns of discolored skin. The disorder is caused by excessive deposits of melanin (normal skin pigment). IP is divided into 4 stages, which frequently overlap or appear together. During the first stage, which begins between birth and 6 months of age, there is inflammation accompanied by skin redness and spiral lines of small fluid-filled blisters. The second stage gradually develops with rough, warty skin growths which appear on the arms or legs and, sometimes, on the head or trunk. These growths, which are often arranged in the same spiral or linear pattern as in the first stage, usually resolve during infancy or early childhood. The third stage begins between 3 months and 2 years of age and is characterized by discolorations appearing in unusual patterns. The fourth stage consists of diminished pigmentation or atrophy in areas of previous discoloration. In rare cases of IP, hair loss with scarring and non-dermatological symptoms such as dental problems (delayed tooth growth or decay, missing or malformed teeth), diminished vision, seizures, muscle spasms, or slight paralysis may occur. Developmental abnormalities including dwarfism or short stature, club foot, spina bifida, skull and ear deformities, cleft lip or palate, atrophy on one side of the body, abnormal development of cartilage, congenital dislocation of hip, incomplete development of one side of the spinal bones, and extra ribs or webbed fingers may occur with the disorder but are not characteristic. In a few cases of IP, extremely wooly or kinky hair and an immune system dysfunction may also appear.

74. Health Library - Incontinentia Pigmenti FREE. incontinentia pigmenti. Self Help Clearinghouse. National IncontinentiaPigmenti Foundation. National network. Founded http://hvlib.integris-health.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc

75. Incontinentia Pigmenti Type 1 incontinentia pigmenti type 1. Examinations PhotographsMovies Links Home Search noJava Home. http://medgen.genetics.utah.edu/photographs/pages/incontinentia_pigmenti_type_1.

incontinentia pigmenti type 1 Examinations Photographs Movies Links ... noJava Home

76. Macular Vasculopathy And Its Evolution In Incontinentia Pigmenti Macular vasculopathy and its evolution in incontinentia pigmenti. Morton F. Goldberg1. PURPOSE To describe macular vasculopathy in incontinentia pigmenti. http://www.szp.swets.nl/szp/journals/og193141.htm

Ophthalmic Genetics 1998, Vol.19, No.3, pp. 141-148 © Æolus Press Research reports Macular vasculopathy and its evolution in incontinentia pigmenti Morton F. Goldberg The Johns Hopkins University School of Medicine and Hospital, Wilmer Ophthalmological Institute, Baltimore, United States of America Keywords: Incontinentia pigmenti , macula , blood vessels , retinal detachment .

77. Incontinentia Pigmenti incontinentia pigmenti. IN THE REST OF THE WORLD. The US Nat'lincontinentia pigmenti Foundation New York (US). http://www.eadv.org/skinweb/incpig.html

78. Incontinentia Pigmenti incontinentia pigmenti. Dermatology Incontinencia pigmenti Dermatology OnlineJournal; incontinentia pigmenti; incontinentia pigmenti; Incontinentia http://www.edae.gr/incontinentia.html

HELLENIC ASSOCIATION DERMATOLOGY - VENEREOLOGY INCONTINENTIA PIGMENTI Dermatology Online Atlas (DOIA) Erlangen: Incontinentia Pigmenti Achromians Familial form of the hereditary form of incontinentia pigmenti (IP2) Incontinentia pigmenti, also known as Bloch-Sulzberger syndrome, is a rare genodermatosis that usually appears at birth or shortly thereafter. The disease is characterized by swirled patterns of hyperpigmentation which is also evident in biopsies of the streaks that show pigment within dermal macrophages ('incontinent pigment'). Associated findings include seizures, mental retardation, strabismus, cataracts, and delayed or impaired dentition. The pigmentary lesions disappear with aging owing to a selection against cells in which the mutation-bearing X chromosome is active. Fundus and Fluorescein Documentation of Hypomelanosis of Ito Tomohiro Ikeda, MD; Keiko Sato, MD; Taku Miyaura, MD Incontinencia pigmenti Dermatology Online Journal Incontinentia pigmenti Incontinentia Pigmenti Incontinentia Pigmenti - 1 Photo, Dermatology ImageBase, Dept. of Dermatology / University of Iowa Incontinentia Pigmenti - 2 Photo, Dermatology ImageBase, Dept. of Dermatology / University of Iowa

79. Incontinentia Pigmenti Medical Information on incontinentia pigmenti. For whom is this informationintended? Medical Information on incontinentia pigmenti. http://www.ssc.mhie.ac.uk/eyeconds/IncPig.htm

80. Incontinentia Pigmenti : Meddie Health Search ITEMS LINKS incontinentia pigmenti Informational sheet compiled byNational Institute of Neurological Disorders and Stroke. (Rating http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/In

HOME ADD A LINK MODIFY A LINK NEW LINKS ... TOP RATED Search Meddie: the entire directory only this category More search options Home Health Conditions and Diseases ... Genetic Disorders : Incontinentia Pigmenti ITEMS: LINKS: Incontinentia Pigmenti Informational sheet compiled by National Institute of Neurological Disorders and Stroke. (Rating: 0.00 Votes: 0) Rate It MCW Healthlink: Incontinentia Pigmenti An article about this rare genetic disorder, its stages and symptoms. (Rating: 0.00 Votes: 0) Rate It National Library of Medicine Bloch-sulzberger syndrome, the synonyms, a summary and major features. (Rating: 0.00 Votes: 0) Rate It Readers Digest Health: IP A general discussion about incontinentia pigmenti, with alternate names and further resources. (Rating: 0.00 Votes: 0) Rate It Vanderbilt Medical Center An article about incotinentia pigmenti. (Rating: 0.00 Votes: 0) Rate It HOME ADD A LINK MODIFY A LINK ... Design © ISC Enterprises Inc.

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