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Incontinentia Pigmenti:     more detail

The Official Parent's Sourcebook on Incontinentia Pigmenti: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11-18 Incontinentia pigmenti: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005 Incontinentia pigmenti may not be that rare.(News): An article from: Pediatric News by Sherry Boschert, 2008-09-01 Incontinentia pigmenti lesions evolve.(Skin Disorders): An article from: Family Practice News by Doug Brunk, 2007-01-15 Incontinentia pigmenti: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005 Incontinentia Pigmenti - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17 Eosinophilic Cutaneous Conditions: Churg-strauss Syndrome, Hypereosinophilic Syndrome, Incontinentia Pigmenti, Eosinophilic Granuloma Incontinentia pigmenti: treatment of IP with topical tacrolimus.(Case study): An article from: Journal of Drugs in Dermatology by Chad J. Jessup, Shane C. Morgan, et all 2009-10-01 Delayed Onychodystrophy of Incontinentia pigmenti: an Evidence-based review of Epidemiology, diagnosis and management.(ORIGINAL ARTICLES)(Clinical report): ... from: Journal of Drugs in Dermatology by Sae-Ryoon Chun, Rashid M. Rashid, 2010-04-01 Incontinentia pigmenti may be staged eruption in infant girls.(Clinical Rounds): An article from: Pediatric News by Doug Brunk, 2007-02-01 Look for incontinentia pigmenti signs.(Clinical Rounds): An article from: Skin & Allergy News by Doug Brunk, 2007-02-01

lists with details

41. Incontinentia Pigmenti
    Article describes incontinentia pigmenti, its symptoms, diagnosis, and treatment.  
    http://rarediseases.about.com/od/rarediseasesi/a/incontinentia05.htm
    
    Extractions: 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); Sign Up Now for the Rare / Orphan Diseases newsletter! 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
    
    Extractions: 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); Sign Up Now for the Rare / Orphan Diseases newsletter! 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

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
    
    Extractions: 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 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
    
    Extractions: 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

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
    
    Extractions: Advanced Search Or click the first letter of a drug name: A B C D ... Z Injury Disease Nutrition Poison ... Incontinentia pigmenti - side Incontinentia pigmenti achromians is a congenital (present at birth) disorder that causes unusual and sometimes bizarre patterns of hypopigmented (diminished pigment) skin. Hypomelanosis of Ito The cause of this disorder is unknown, though most patients have abnormal chromosomes. Girls are affected slightly more often than boys. 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
    
    Extractions: Advanced Search Or click the first letter of a drug name: A B C D ... Z Injury Disease Nutrition Poison ... Incontinentia pigmenti on the leg Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Bloch-Sulzberger's disease 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
    
    Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: 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
    
    Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation 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.

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
    
    Extractions: low graphics 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

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
    
    Extractions: 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
    
    Extractions: 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

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
    
    Extractions: 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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