41. Incontinentia Pigmenti Article describes incontinentia pigmenti, its symptoms, diagnosis, and treatment. http://rarediseases.about.com/od/rarediseasesi/a/incontinentia05.htm

var zLb=12; var zIoa1 = new Array('Suggested Reading','Hypomelanosis of Ito','http://rarediseases.about.com/od/rarediseasesh/a/hypomelanoito05.htm','About Skin Conditions: Vitiligo','http://dermatology.about.com/od/vitiligo/'); var zIoa2 = new Array('Elsewhere on the Web','Incontinentia Pigmenti International Foundation','http://imgen.bcm.tmc.edu/IPIF/','NINDS: Incontinentia Pigmenti','http://www.ninds.nih.gov/disorders/incontinentia_pigmenti/incontinentia_pigmenti.htm'); zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases I - L Rare Diseases: I Incontinentia Pigmenti Rare Diseases Essentials Rare Diseases: Basic Information Rare Diseases Support Groups ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Stay up to date! Compare Prices Email to a friend ... Print this page Suggested Reading Hypomelanosis of Ito About Skin Conditions: Vitiligo Elsewhere on the Web Incontinentia Pigmenti International Foundation NINDS: Incontinentia Pigmenti Most Popular Muscular Dystrophy ALD and Lorenzo's Oil Progeria Syndromes Leprosy (Hansen's Disease) ... The Elephant Man What's Hot Muscular Dystrophy Autoimmune Kidney Disease Minamata Disease Charcot-Marie-Tooth Disease ... Meckel-Gruber Syndrome adunitCM(150,100,'x55')

42. Incontinentia Pigmenti This Xlinked genetic disorder, sometimes termed Bloch-Sulzberger syndrome, may cause neurological problems, serious eye disorders, tooth abnormalities, http://rarediseases.about.com/b/a/184696.htm

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Incontinentia Pigmenti Rare/Orphan Diseases Blog Main From Mary Kugler Your Guide to Rare / Orphan Diseases FREE Newsletter. Sign Up Now! July 10, 2005 Incontinentia Pigmenti This X-linked genetic disorder, sometimes termed Bloch-Sulzberger syndrome, may cause neurological problems, serious eye disorders, tooth abnormalities, and unique skin lesions and pigmentation. Incontinentia pigmenti may also occur with Klinefelter syndrome. Email to a Friend Display Latest Headlines Read Archives powered by Movable Type Advertisement Most Popular Muscular Dystrophy ALD and Lorenzo's Oil Progeria Syndromes Leprosy (Hansen's Disease) ... The Elephant Man What's Hot Muscular Dystrophy Autoimmune Kidney Disease Minamata Disease Charcot-Marie-Tooth Disease ... Meckel-Gruber Syndrome adunitCM(150,100,'x55')

43. Short Description Of Cell Lines. Pathology: Incontinentia Pigmenti *308300 Version 4.200205. Short description of cell lines. Pathology incontinentia pigmenti *308300 OMIM record. By selecting the cell line name, http://www.biotech.ist.unige.it/cldb/pat20.html

Version Short description of cell lines. Pathology: incontinentia pigmenti OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser human, Caucasian skin, fibroblast PVCGU By Beatrice...

44. ORPHANET - Maladies Rares - Médicaments Orphelins incontinentia pigmenti (IP) est un trouble de la pigmentation transmis de manière http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=464

45. AllRefer Health - Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease) incontinentia pigmenti Syndrome (BlochSulzberger s Disease) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, http://health.allrefer.com/health/incontinentia-pigmenti-syndrome-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Incontinentia Pigmenti Syndrome Incontinentia Pigmenti Syndrome Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Alternate Names : Bloch-Sulzberger's Disease Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Incontinentia Pigmenti on the Leg Incontinentia Pigmenti on the Leg Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear.

46. AllRefer Health - Incontinentia Pigmenti Achromians (Hypomelanosis Of Ito) incontinentia pigmenti Achromians (Hypomelanosis of Ito) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, http://health.allrefer.com/health/incontinentia-pigmenti-achromians-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Incontinentia Pigmenti Achromians Incontinentia Pigmenti Achromians Definition Treatment Expectations or Prognosis Complications ... Go To Main Page Alternate Names : Hypomelanosis of Ito Definition Incontinentia pigmenti achromians is a congenital disorder that causes unusual and sometimes bizarre patterns of hypopigmented (diminished pigment) skin. Incontinentia Pigmenti - Side The cause of this disorder is unknown, though most patients have abnormal chromosomes. Girls are affected slightly more often than boys. Previous Top Next Jump to another section Definition Treatment Prognosis Complications ... Calling Your Health Care Provider Topics that might be of interest to you Mental Retardation Scoliosis Strabismus Other Topics Excessive or Unwanted Hair in Women Rashes Seizures Skin Color - Patchy Review Date : 10/27/2003 Main Page of Incontinentia Pigmenti Achromians From Our Sponsors: A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's

47. DermIS / Main Menu / DOIA / Incontinentia Pigmenti / Images incontinentia pigmenti / images. images for the diagnosis incontinentia pigmenti . Click to enlarge. Click to enlarge. Click to enlarge. http://www.dermis.net/doia/diagnose.asp?zugr=d&lang=e&diagnr=757361&topic=t

48. DermIS / Main Menu / DOIA / Incontinentia Pigmenti / Images / Enlarged image incontinentia pigmenti / images / enlarged image. image for the diagnosis incontinentia pigmenti . previous image http://www.dermis.net/doia/image.asp?zugr=d&lang=e&cd=56&nr=54&diagnr=757361

49. Incontinentia Pigmenti Achromians Medical Information incontinentia pigmenti achromians Information from Drugs.com. http://www.drugs.com/enc/incontinentia_pigmenti_achromians.html

Home New Drugs Latest News Drug Interactions ... Forum Drugs.com - prescription drug and medicine information available on over 24,000 approved- medications and pharmaceuticals, including side effects and drug interactions. Log-in Register Advertisement Buy a Link Now Special Offers From our sponsors Categories Diabetes Gastro Center Weight Loss AIDS/HIV ... Sexual Health Advertisement Advanced Search Or click the first letter of a drug name: A B C D ... Z Incontinentia pigmenti achromians Injury Disease Nutrition Poison ... Incontinentia pigmenti - side Incontinentia pigmenti achromians Definition Incontinentia pigmenti achromians is a congenital (present at birth) disorder that causes unusual and sometimes bizarre patterns of hypopigmented (diminished pigment) skin. Alternative Names Hypomelanosis of Ito Causes The cause of this disorder is unknown, though most patients have abnormal chromosomes. Girls are affected slightly more often than boys. Symptoms Streaked, whirled or mottled areas of hypopigmentation   on limbs and trunk Varying degrees of retardation Seizures Crossed eyes (strabismus) Increased body hair ( hirsutism Scoliosis Exams and Tests A Wood's lamp examination of the skin lesions may help confirm the diagnosis. Your doctor may also recommend chromosome analysis or a further medical workup to discover any related medical problems.

50. Incontinentia Pigmenti Syndrome Medical Information incontinentia pigmenti syndrome Information from Drugs.com. http://www.drugs.com/enc/incontinentia_pigmenti_syndrome.html

Home New Drugs Latest News Drug Interactions ... Forum Drugs.com - prescription drug and medicine information available on over 24,000 approved- medications and pharmaceuticals, including side effects and drug interactions. Log-in Register Advertisement Buy a Link Now Special Offers From our sponsors Categories Diabetes Gastro Center Weight Loss AIDS/HIV ... Sexual Health Advertisement Advanced Search Or click the first letter of a drug name: A B C D ... Z Incontinentia pigmenti syndrome Injury Disease Nutrition Poison ... Incontinentia pigmenti on the leg Incontinentia pigmenti syndrome Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Alternative Names Bloch-Sulzberger's disease Causes Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough bumps. Eventually, these bumps clear but leave damaged, hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear. Most people with IPS also have other problems including abnormal teeth

51. MedlinePlus Medical Encyclopedia: Incontinentia Pigmenti Syndrome incontinentia pigmenti syndrome is an inherited disorder that causes incontinentia pigmenti syndrome (IPS) is inherited as a dominant Xlinked trait. http://www.nlm.nih.gov/medlineplus/ency/article/001583.htm

@import url(/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Incontinentia pigmenti syndrome Contents of this page: Illustrations Alternative names Definition Causes, incidence, and risk factors ... Prevention Illustrations Incontinentia pigmenti on the leg Incontinentia pigmenti on the leg Alternative names Return to top Bloch-Sulzberger's disease Definition Return to top Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Causes, incidence, and risk factors Return to top Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear. Most people with IPS also have other problems including abnormal teeth

52. MedlinePlus Medical Encyclopedia: Incontinentia Pigmenti On The Leg incontinentia pigmenti on the leg. incontinentia pigmenti produces darklypigmented swirling marks on the skin. It occurs more frequently in females. http://www.nlm.nih.gov/medlineplus/ency/imagepages/2861.htm

@import url(/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Incontinentia pigmenti on the leg 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. Update Date: 1/17/2004 Updated by: Michael Lehrer, M.D., Department of Dermatology, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network. Home Health Topics Drug Information Encyclopedia ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Page last updated: 18 August 2005

53. Incontinentia Pigmenti Definition - Medical Dictionary Definitions Of Popular Me Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=3964

54. Syndrome, Incontinentia Pigmenti Definition - Medical Dictionary Definitions Of Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=5637

55. Incontinentia Pigmenti NINDS incontinentia pigmenti information page. This Web resource on incontinentia pigmenti (also known as BlochSulzberger Syndrome) is produced by the http://omni.ac.uk/browse/mesh/D007184.html

low graphics Incontinentia Pigmenti other: Dermatitis, Atopic Ehlers-Danlos Syndrome Epidermolysis Bullosa NINDS : incontinentia pigmenti information page This Web resource on incontinentia pigmenti (also known as Bloch-Sulzberger Syndrome) is produced by the National Institute of Neurological Disorders and Stroke (NINDS). A description of incontinentia pigmenti is provided, and available treatments, prognosis, and current research activities are all discussed. Links to related organisations are provided. This resource has a US focus. Patient Education Handout [Publication Type] Incontinentia Pigmenti Last modified: 09 Sep 2005

56. Neurocutaneous Disorders The hallmark of incontinentia pigmenti (BlochSulzberger syndrome) in the neonatal period is the presence of an erythematous vesicular rash. http://pediatricneuro.com/alfonso/pg298.htm

MainMenu Back Next Index INCONTINENTIA PIGMENTI Figure 298.1. Vesicular rash. Typical cutaneous manifestation of incontinentia pigmenti in neonates. Neonates with incontinentia pigmenti should undergo ophthalmological evaluation for retinal dysplasia, uveitis, keratitis, cataracts, and retrolental dysplasia. Incontinentia pigmenti occurs in females. Incontinentia pigmenti is transmitted as an X-linked trait and is lethal in homozygous males. The gene loci are Xp11 (sporadic) and Xp28 (familial). Prenatal diagnosis is possible by DNA analysis. Males born with lesions of incontinentia pigmenti should have chromosomal studies to determine if an XXY karyotype is present. MainMenu Back Next Index

57. Incontinentia Pigmenti incontinentia pigmenti (IP) is a rare genetic dermatological disorder affecting the skin, hair, teeth, http://my.webmd.com/hw/raising_a_family/nord409.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Incontinentia Pigmenti Important It is possible that the main title of the report Incontinentia Pigmenti is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Bloch-Siemens-Sulzberger Syndrome Bloch-Sulzberger Syndrome IP Bloch-Siemens Incontinentia Pigmenti Melanoblastosis Cutis Linearis Pigmented Dermatosis, Siemens-Bloch type Disorder Subdivisions None General Discussion Incontinentia Pigmenti (IP) is a rare genetic dermatological disorder affecting the skin, hair, teeth, and central nervous system. Progressive skin changes occur in four stages, the first of which appears in early infancy or is present at birth. IP is inherited as an X-linked dominant trait. Resources March of Dimes Birth Defects Foundation 1275 Mamaroneck Avenue White Plains, NY 10605

58. Incontinentia Pigmenti incontinentia pigmenti is an Xlinked dominant disorder that presents in at or soon after 4 Congenital herpes simplex can mimic incontinentia pigmenti, http://dermatology.cdlib.org/DOJvol4num1/path/incont2.html

DOJ Index Spanish Portuguese Answer: Incontinentia Pigmenti Figure 3 Figure 4 Skin biopsy demonstrating marked edema of the upper epidermis Epidermal spongiosis and an eosinophil-rich cellular infiltrate Histologically, there is spongiosis manifest as epidermal intercellular edema with exocytosis of numerous eosinophils and mononuclear cells both within the epidermis as well as in spongiotic foci. Dyskeratotic keratinocytes are present adjacent to spongiotic microvesicles. An interstitial infiltrate of lymphocytes and eosinophils is present in the papillary dermis. Incontinentia pigmenti is an X-linked dominant disorder that presents in at or soon after birth. Although the condition involves the skin primarily, there are a number of associated disorders including dental defects, convulsive disorders, mental retardation, ocular abnormalities and childhood neoplasms. Because it is almost always lethal in males, is observed almost exclusively in female infants. Three successive stages of the cutaneous disease have been described. The first stage is characterized by a linear, erythematous, vesiculobullous eruption on the trunk and extremities within the first 2 weeks of life.[2] Histologically, spongiosis containing numerous eosoinophils with abundant dyskeratotic keratinocytes is noted.[1,3] The second stage, the so-called verrucous stage, usually develops within a few weeks and is manifest as verrucous hyperkeratotic papules and plaques. [2] Microscopically, there is acanthosis, papillomatosis, and hyperkeratosis with abundant dyskeratotic cells, often in small whorls in the epidermis.[3] Vacuolar change of the basal layer may be noted. Finally, as lesions resolve, the hyperpigmented stage develops in which there is a whorled slate-gray to brown hyperpigmentation that usually fades with time.[2] These areas contain many melanophages in the upper dermis.[3]

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

60. Show-documents.asp incontinentia pigmenti Written Information. Care Treatment. incontinentia pigmenti New Search Contact Us Disclaimer Send This Link http://www.clevelandclinic.org/health/search/do-query.asp?TopicId=1312

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