81. Arch Dermatol -- Abstract: Incontinentia Pigmenti. A World Statistical Analysis, incontinentia pigmenti. A world statistical analysis. RG Carney. incontinentia pigmenti (BlochSulzberger syndrome) is an uncommon genodermatosis that http://archderm.ama-assn.org/cgi/content/abstract/112/4/535

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 112 No. 4, April 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Carney RG Articles that cite this article Contact me when this article is cited Incontinentia pigmenti. A world statistical analysis R. G. Carney Incontinentia pigmenti (Bloch-Sulzberger syndrome) is an uncommon genodermatosis that usually affects female infants. I reviewed 464 references from the world literature and found 653 apparently valid reports of patients with incontinentia pigmenti. Skin manifestations were found to be somewhat more common than previously reported, and systemic manifestations were found in 79.8% of the patients.

82. Incontinentia Pigmenti Hyperpigmented macules of incontinentia pigmenti. , Skin in incontinentia pigmenti (1) incontinentia pigmenti International Foundation. About Links http://www.medlink.com/PublicCIP.ASP?access=public&UID=MLT0002S&code=

83. Incontinentia Pigmenti Achromiens - Definition Of Incontinentia Pigmenti Achromi Definition of incontinentia pigmenti achromiens in the Medical Dictionary and Thesaurus. incontinentia pigmenti achromiens explanation. http://medical-dictionary.thefreedictionary.com/incontinentia pigmenti achromien

Domain='thefreedictionary.com' word='incontinentia pigmenti achromiens' Your help is needed: American Red Cross The Salvation Army join mailing list webmaster tools Word (phrase): Word Starts with Ends with Definition subscription: Dictionary/ thesaurus Computing dictionary Medical dictionary Legal dictionary Financial dictionary Acronyms Columbia encyclopedia Wikipedia encyclopedia Hutchinson encyclopedia incontinentia pigmenti achromiens 0.03 sec. Page tools Printer friendly Cite / link Email Feedback incontinentia pigmenti a·chro·mi·ens -kr m ns) n. An inherited skin disorder characterized by the appearance of macules with less than normal pigmentation in a swirling or marble pattern, and associated with other abnormalities of the nerves, eyes, muscles, and bones. Also called hypomelanosis of Ito Mentioned in No references found Medical browser Full browser incomplete fistula incomplete foot presentation incomplete fracture inconstant ... incontinentia pigmenti incontinentia pigmenti achromiens incoordination increment incretion incrustation ... incontinentia pigmenti incontinentia pigmenti achromiens Incontinently Incontracted incontro improvviso, L'

84. AJNR -- Sign In Page Summary incontinentia pigmenti is a rare neurocutaneous disorder that may incontinentia pigmenti should be included in the differential diagnosis of http://www.ajnr.org/cgi/content/full/26/6/1580

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to American Journal of Neuroradiology Online. Full Text Diffuse Cortical Necrosis in a Neonate with Incontinentia Pigmenti and an Encephalitis-Like... Wolf et al. AJNR Am J Neuroradiol. This Article Abstract Figures Only Full Text (PDF) ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Wolf, N. I. Articles by Rating, D. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 7 days for US$10.00 Pay for Admission - You may access all content in American Journal of Neuroradiology Online (from the computer you are currently using) for 7 days for US$25.00.

85. Incontinentia Pigmenti : Sites Et Documents Francophones incontinentia pigmenti type 2 . IPF - association incontinentia pigmenti France http://www.chu-rouen.fr/ssf/pathol/incontinentiapigmentia.html

Incontinentia pigmenti Synonyme(s) CISMeF incontinentia pigmenti type 1 ; incontinentia pigmenti type 2 . Synonyme(s) MeSH Bloch Sulzberger, syndrome ; Dermatose pigmentaire éclaboussures ; Naevus chromatophore héréditaire ; Syndrome de Bloch Sulzberger Ne pas confondre avec troubles de la pigmentation Arborescence(s) incontinentia pigmenti incontinentia pigmenti maladies de la peau et du tissu conjonctif maladies et malformations congénitales, héréditaires et néonatales Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : patient Incontinentia pigmenti [Par Dr Blanchet-Bardon C. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; signes de la maladie, sites internet, dysmorphologie, conseil génétique, génodermatoses, laboratoires de diagnostic, projets de recherche en cours, associations de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2002 ; visité le : 17/09/2003]. mots clés : conseil génétique *incontinentia pigmenti incontinentia pigmenti /diagnostic maladies rares ... signes et symptômes type : *association patients *structure recherche *texte IPF - association Incontinentia Pigmenti France [Site éditeur

86. Incontinentia Pigmenti : Arborescences MeSH http://www.chu-rouen.fr/navimesh/I/naviincontinentiapigmenti.html

Incontinentia pigmenti : arborescences MeSH Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF maladies et malformations congénitales, héréditaires et néonatales malformations malformations multiples Alagille, syndrome ... xeroderma pigmentosum 25 février 2005 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

87. Incontinentia Pigmenti incontinentia pigmenti is a systemic disease affecting many ectodermal tissues. incontinentia pigmenti is an Xlinked dominant disease. http://www.kfshrc.edu.sa/annals/205_206/00-070.htm

Incontinentia Pigmenti Sultan Al-Khenaizan, MBBS, FRCPC Incontinentia pigmenti (IP) is an X-linked dominant (XLD) disorder that was first described in 1906 by Garrod, and subsequently named after Bloch and Sulzberger. The skin lesions in IP follow four well-characterized successive stages: vesicular, verrucous, whorl or streak-like hyperpigmentation, and hypopigmented scars. Skin appendages, including hair and teeth are commonly affected in IP, with scarring alopecia and peg-shaped teeth. IP also affects many other body systems, most commonly the central nervous system (CNS) and the eyes. Almost all patients with IP are females because of the lethality of the disease in males. Case Report From the Department of Medicine, King Fahad National Guard Hospital, Riyadh, Saudi Arabia. leaving no marks. The rest of the physical examination was unremarkable. Skin examination of the mother revealed multiple white, hypopigmented atrophic swirls and streaks along the Blaschko lines. Mouth examination revealed hypodontia and conical widely spaced teeth. The diagnosis of incontinentia pigmenti was made. CT scan and MRI of the brain revealed no abnormality. Electroencephalogram study was normal and there were no more seizures. The infant was discharged home in good condition on oral phenobarbitol. At three months' follow-up, the pigmentation had extended to most of the lower extremities and sides of the trunk (Figure 1), with no other skin changes. Neurological examination by the neurologist was normal.

88. Incontinentia Pigmenti Articles, Support Groups, And Resources incontinentia pigmenti articles, support groups, and resources for patients from Med Help International (www.medhelp.org) http://www.medhelp.org/HealthTopics/Incontinentia_Pigmenti.html

[Health Topics A-Z] A B C D ... Z Incontinentia Pigmenti Support Groups: Incontinentia Pigmenti International Foundation Med Help International Search Medical Forums / Message Boards ... Site Map Revised: 9/7/2005

89. Hemihypertrophy And Primary Small Intestinal Lymphangiectasia In Incontinentia P incontinentia pigmenti achromians (IPA), also known as hypomelanosis of Ito, Hypomelanosis of Ito (incontinentia pigmenti achromians) Report of three http://www.ijppediatricsindia.org/article.asp?issn=0019-5456;year=2004;volume=71

90. DermIS / Main Menu / PeDOIA / Table Of Contents / 2 Genodermatoses / 2.9 Neuro information on the diagnosis incontinentia pigmenti Achromians The term hypomelanosis of Ito (incontinentia pigmenti achromians) has been used as a http://dermis.multimedica.de/doia/diagnose.asp?zugr=p&lang=e&diagnr=757362&topic

91. DermIS / Main Menu / PeDOIA / Table Of Contents / 2 Genodermatoses / 2.9 Neuro / table of contents / 2 Genodermatoses / 2.9 Neurocutaneous Syndromes / 2.9.2 incontinentia pigmenti. images for the diagnosis incontinentia pigmenti http://dermis.multimedica.de/doia/diagnose.asp?zugr=p&lang=e&diagnr=757361&topic

92. Incontinentia Pigmenti Survival of Male Patients with incontinentia pigmenti Carrying a Lethal Mutation Can incontinentia pigmenti Left medial thigh - 1 week old baby girl http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=161

93. INCONTINENTIA PIGMENTI incontinentia pigmenti-Left Upper Leg-1 week old baby girl) http://digilander.libero.it/camdic/INCPIG.html

INCONTINENTIA PIGMENTI Prof. Camillo O. DI CICCO Member of " DNA REPAIR INTEREST GROUP " ( NIH ) National Insitutes of Health, Bethesda 3td EUROSKIN Conference - Stockholm, Sweden La sintomatologia cutanea, nella sua forma classica evolve in tre stadi: I° STADIO con presenza di lesioni di tipo eritemato-vescico-bolloso a gittate successive, disposizione lineare ed interessamento del tronco e degli arti; presente, inoltre, ipereosinofilia ematica. II° STADIO si evidenzia tra la seconda e la sesta settimana di vita con lesioni papulo lichenoidi, ipercheratosiche, verrucose, con aspetto di strie allungate nella parte distale degli arti (ginocchio, dorso del piede e della mano). III° STADIO al 3°- 6° mese di vita compaiono macule pigmentate brune a livello del tronco con disposizione a vortice, a turbine, a schizzi. Tale cronologia può non essere rispettata ed inoltre non è chiarito il rapporto tra il susseguirsi delle lesioni. - Anomalie neurologiche nel 30% dei casi, con interessamento motorio-spastico, convulsioni, deficit intellettivo. - Anomalie oculari nel 35% dei casi, con cecità nel 7,5% (cataratta, retinite, uveite, atrofia del nervo ottico).

94. Orthodontic And Orthopedic Treatment Of A Patient With Incontinentia Pigmenti Abstract incontinentia pigmenti is an uncommon, inherited disorder with Key Words incontinentia pigmenti, Partial anodontia, Rapid maxillary expansion http://www.angle.org/anglonline/?request=get-document&issn=0003-3219&volume=073&

95. Case Report: Orthodontic Treatment Of Dental Problems In Incontinentia Pigmenti Abstract incontinentia pigmenti is an uncommon genodermatosis that occurs in This report describes a patient with incontinentia pigmenti who exhibited http://www.angle.org/anglonline/?request=get-abstract&issn=0003-3219&volume=068&

96. Incontinentia Pigmenti Achromians incontinentia pigmenti side incontinentia pigmenti - side. incontinentia pigmenti achromians. Definition. A congenital disorder that causes unusual and http://www.shands.org/health/information/article/001461.htm

Disease Injury Nutrition Poison ... Incontinentia pigmenti - side 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. Symptoms: streaked, whirled or mottled areas of hypopigmentation (limbs and trunk) varying degrees of retardation seizures crossed eyes strabismus increased body hair ( hirsutism scoliosis Signs and tests: A Wood's lamp examination of the skin lesions may help confirm the diagnosis. Your physician may also recommend chromosome analysis or a further medical workup to discover any associated medical problems. Treatment: There is no treatment for the hypopigmentation . Treatment consists of treating the symptoms. Cosmetics or clothing may be used to cover the hypopigmented spots if desired. Seizures scoliosis , and other problems are treated as necessary.

97. UNTSHC Clinic Digital Library incontinentia pigmenti List of documents; incontinentia pigmenti Achromians List of incontinentia pigmenti (Keyword search) List of documents http://unthsc-dl.slis.ua.edu/clinical/dermatology/pigmentation/hyperpigmentation

Clinical Resources by Topic: Dermatology Incontinentia Pigmenti Clinical Resources Pediatrics Atlases News Miscellaneous Resources See also: Dermatological Clinical Procedure Resources General Dermatology Clinical Resources Incontinentia Pigmenti Patient/Family Resources Harrison's Principles of Internal Medicine 16th Ed.-2005: Table of contents Lewis Library subscription INFO Chapter 46. Approach to the Patient with a Skin Disorder: Table of contents Introduction: Access document Approach to the Patient: Access document Diagnostic Techniques: Access document Further Reading: Access document Chapter 48. Skin Manifestations of Internal Disease: Table of contents Introduction: Access document Hyperpigmentation: Access document Further Reading: Access document Yanoff: Ophthalmology 2nd Ed.-2004 (MD Consult): Table of contents Lewis Library subscription INFO Chapter 36 - Cataract Formation Mechanisms: Access document Chapter 122 - Proliferative Retinopathies Access document Ferri: Ferri's Clinical Advisor: Instant Diagnosis and Treatment - 2005 (MD Consult): Table of contents Lewis Library subscription INFO Section II - Differential Diagnosis Hyperpigmentation: Access document Goldman: Cecil Textbook of Medicine 22nd Ed.-2004 (MD Consult):

98. VulgarisMedical - Encyclopédie || Incontinentia Pigmenti Translate this page incontinentia pigmenti. Anglais incontinentia pigmenti. Dernière modification 23/06/2004. Synonyme(s) Bloch-Sulzberger (maladie ou syndrome de), http://www.vulgaris-medical.com/front/?p=index_fiche&id_article=5244

99. Incontinentia Pigmenti - Små Och Mindre Kända Handikappgrupper incontinentia pigmenti beskrevs första gången 1926 av Bloch. Vid incontinentia pigmenti fungerar inte genen och dess motsvarande äggviteämne. http://www.sos.se/smkh/1997-29-025/1997-29-025.htm

Socialstyrelsen 106 30 Stockholm Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper Incontinentia pigmenti Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik ... Databasreferenser Dokumentdatum: 2001-04-03 HTML-version 2.0 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Stadium 1: Stadium 2 Stadium 3 tadium 4 Diagnostik Praktiska tips Resurspersoner birgitta.bergendal@odont.ltjkpg.se Kurser, erfarenhetsutbyte, rekreation ip_patforening@hotmail.com

100. Incontinentia Pigmenti incontinentia pigmenti Michigan Genetic Support Groups; incontinentia pigmenti National Institutes of Health, Bethesda, Maryland 20892 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

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