81. Welcome To AJC! Incontinentia pigmenti syndrome See images. Overview Symptoms Treatment Prevention. Alternative names blochsulzberger s disease. Definition http://www.ajc.com/health/healthfd/shared/health/adam/ency/article/001583.html

Main Contact us Edit profile Subscribe ... Register Now It's Free! Log in E-mail preferences Site Index Search: Site Yellow Pages Customer care ajc.com Nation/World Metro ... Personals ajc services Archives Advertise online Advertise in print Obituaries ... Sitemap Print edition Today This week A1 image E-mail News  Sign up for our  FREE newsletters: News Sports Business Travel Deals ... Logged in? ajc store Gifts Photos/pages Browser tip  Make ajc.com  your homepage: ajc guides Schools Visitors Illustrated Health Encyclopedia Important notice Ency. home Disease I Incontinentia pigmenti syndrome See images Overview Symptoms Treatment ... Prevention Alternative names: Bloch-Sulzberger's disease Definition: An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Causes and Risks 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

82. Veröffentlichungen Von Universitätsangehörigen Translate this page Jurin-Bunte, Bernadette - ua Incontinentia pigmenti (bloch-sulzberger-syndrome) Case Report and Differential Diagnosis to Related Dermato-Ocular syndromes. http://www.uni-saarland.de/z-einr/ub/uni-veroeff/B99/f4_2.htm

Jahresbibliographie 1999 FR 4.2 - Augenheilkunde (29.05.00) Bohlender, Tanja - u.a.: Patientendarstellung: Malignes Melanom der Karunkel. - In: Klin. Mbl. Augenheilkd, 215 (1999), Suppl. 9, 9 Gantenbein, Claude - u.a.: An oculocutaneous presentation of essential progressive telangiectasia. - In: British Journal of Dermatology, 140 (1999), S. 969-970 Hille, Konrad Jurin-Bunte, Bernadette - u.a.: Incontinentia pigmenti (Bloch-Sulzberger-Syndrome): Case Report and Differential Diagnosis to Related Dermato-Ocular Syndromes. - In: Ophthalmologica, 213 (1999), S. 63-69 Krause, Mathias - u.a.: Ablation of Vitreous Tissue with Erbium: YAG-Laser. - In: Invest. Ophthalmol. Vis. Sci, 40 (1999), S. 1025-1032 - u.a.: Sharp or blunt tipped needles for retrobulbar anaesthesia. - In: Anaesthesia, 54 (1999), S. 86 Palmowski, Anja Pfau, Britta - u.a.: Ocular Changes in Mucopolysaccharidosis IV A (Morquio A Syndrome) and Long-Term Results of Perforating Keratoplasty. - In: Ophthalmologica, 213 (1999), S. 200-215 Ruprecht, Klaus Wilhelm Scherer, Volker

83. Incontinentia Pigmenti : Sites Et Documents Francophones syndrome Bloch Sulzberger . http://www.chu-rouen.fr/ssf/pathol/incontinentiapigmentia.html

Incontinentia pigmenti Menu général CISMeF Synonyme(s) CISMeF incontinentia pigmenti type 1 ; incontinentia pigmenti type 2 . Synonyme(s) MeSH Bloch Sulzberger, syndrome ; Dermatose pigmentaire éclaboussures ; Naevus chromatophore héréditaire ; Syndrome Bloch Sulzberger Ne pas confondre avec troubles pigmentation Arborescence(s) incontinentia pigmenti incontinentia pigmenti maladies et malformations congénitales, héréditaires et néonatales maladies peau et tissu conjonctif 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 ... signes et symptômes type(s) : * texte structure recherche association patients IPF - association Incontinentia Pigmenti France [Site éditeur

84. GASNet Anesthesiology: Contents S - Z Sturge. Sturge Weber syndrome. Sulzberger. Bloch - Sulzberger syndrome. Sydenham. Sydenham s Chorea. System Lupus Erythematous. System Lupus Erythematous. Tangier. http://www.gasnet.org/pediatric-syndromes/s2z_br.php

Contents S - Z - pediatric syndromes - Sachs Tay - Sachs Disease Saethre Saetre - Chotzen Syndrome Sanfilippo Sanfilippo Syndrome (Mucopolysaccharidosis Type III) Scheie Scheie Disease (Mucopolysaccharidosis Type V) Schönberg Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Schönlein Henoch - Schönlein Purpura Schuller Hand - Schuller - Christian Disease (Histiocytosis X) Schwartz Schwartz - Jampel Syndrome Scleroderma Scleroderma Senior Senior - Loken Syndrome Seip Seip - Lawrence Syndrome Sheldon Freeman - Sheldon Syndrome (Whistling Face Syndrome) Shone Shone Syndrome Shy Shy - Drager Syndrome Siemens Christ - Siemens - Touraine Syndrome (Anhydrotic Ectodermal Dysplasia) Silver Russell - Silver Syndrome Sipple Sipple's Syndrome (MEN - type II) Siwe Letterer - Siwe Disease (Acute Disseminated Histiocytosis) Smith Smith - Lemli - Opitz Syndrome Sotos Sotos's Syndrome (Cerebral Gigantism) Spatz Hallervorden - Spatz Disease Stevens Erythema Multiforme Major (Stevens - Johnson Syndrome) Steinert Myotonic Dystrophy (Steinert's Disease) Stickler Stickler Syndrome Still Still's Disease Strandberg Groenblad - Strandberg Syndrome (Pseudoxanthoma Elasticum) Streiff Hallerman - Streiff Syndrome Sturge Sturge - Weber Syndrome Sulzberger Bloch - Sulzberger Syndrome Sydenham Sydenham's Chorea System Lupus Erythematous System Lupus Erythematous Tangier Tangier Disease (Analphalipoproteinemia) TAR TAR Syndrome (Thrombocytopenia and Absent Radius) Tauri Tauri Disease (Glygogen Storage Disease Type VII) Tay Tay - Sachs Disease Taybi Rubenstein - Taybi Syndrome Telangiectasia

85. Siemens' Syndrome I (www.whonamedit.com) First described by Lechleuthner and Siemens in 1925, this syndrome resembles incontinentia pigmenti (Bloch Sulzberger syndrome). http://www.whonamedit.com/synd.cfm/1057.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Siemens' syndrome I Also known as: Touraine’s polykeratosis Synonyms: Congenital ectodermal defect syndrome, congenital polykeratosis, follicularis syndrome, ichtyosis congenita, Keratosis follicularis acneiformis Typ Siemens (German), keratosis follicularis spinulosa decalvans, keratosis follicularis spinulosa decalvans cum ophiasis, keratosis multiformis, keratosis multiformis idiopathica Siemens, melanosis corii degeneration, melanosis corii degenerativa (Siemens). Associated persons: Hermann Werner Siemens Albert Touraine Description: A familial form of keratosis present from birth. It involves the face, neck, forearms, ears, palms and soles, and backs of the hands, and is associated with loss of the eyebrows, eyelashes, and beard, thickening of the eyelids, blepharitis, ectropion, and corneal abnormalities (punctate lesions). Photophobia and lacrimation are the early symptoms. Only males show the complete picture, the heterozygotous carriers, partial expression. Inheritance is X-linked, but autosomal dominant transmission has also been reported.

86. Birth Disorder Information Directory - I Perineoscrotal Hypospadias. Incontinentia Pigmenti (IP, Bloch Sulzberger syndrome) List of Sites. Indifference to Pain (Congenital Analgesia) http://www.bdid.com/defecti.htm

HOME I I-Cell Disease (Mucolipidosis, Type II) List of Sites ICE Syndrome (Ichthyosis-Cheek-Eyebrow Syndrome, Sidransky Feinstein Goodman Syndrome) ICHTHYOSISCHEEKEYEBROW SYNDROME ICF Syndrome See Centromeric Instability Immunodeficiency Syndrome Ichthyosiform/Ichthyosis List of Sites -Alopecia-Eclabion-Ectropion-Mental Retardation Syndrome ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION -Camptodactyly Syndrome See Camptodactyly-Ichthyosis Syndrome -Cheek-Eyebrow Syndrome See ICE Syndrome -Hepatosplenomegaly-Cerebellar Degeneration Syndrome ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION -Spastic Neurologic Disorder-Oligophrenia Syndrome See Sjogren-Larsson Syndrome with Large Keratohyalin Granules in the Skin ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN Erythroderma -Corneal Involvement-Deafness Syndrome See KID Syndrome Congenital (Brocq) Also see Netherton Syndrome Bullous Form (Epidermolytic Hyperkeratosis) Bullous ichtyosiform erythroderma congenita BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ Nonbullous Form Type 1 (Nonbullous Congenital Ichthyosiform Erythroderma, Type I)

87. Encyclopedia B-Bm (Search FastHealth.com) Encyclopedia B-Bm Blepharitis Blepharoplasty Blepharospasm Blind loop syndrome Blindness Blindness temporary Blisters Bloating Bloch Sulzberger syndrome Blocked lacrimal duct http://www.fasthealth.com/encyclopedia/encyclopedia_B-Bm.php

Email This! A-Am An-Az B-Bm ... Z B-Bm Babinskis reflex Baby care Baby rash Bacitracin overdose ... Dead Links

88. DEUTSCH-SPRACHIGE OPHTHALMOPATHOLOGEN (DOP): Originalbeiträge 1999 Bloch - Sulzberger syndrome). http://dog-patho.dog.org/abstract99/dop_24.html

DOP Originalbeiträge XXVII. Jahrestagung der Deutschsprachigen Ophthalmopathologen (DOP) am 21. und 22. September 1999, Universitäts Krankenhaus Eppendorf Incontinentia pigmenti U. Schaudig Universitäts Krankenhaus Eppendorf Augenklinik und Poliklinik Martinistrasse 52 20246 Hamburg Hist. Nr.: 19150 Klinische Vorgeschichte: Augenärztliche Erstuntersuchung des Kindes im Alter von 17 Monaten bei eitriger Konjunktivitis. Unkomplizierte Schwangerschaft und Geburt im Gestationsalter von 38 Wochen. Pigmentflecken am Stamm. Pädiatrischerseits sonst keine Besonderheiten. Incontinentia pigmenti bei der älteren Schwester bekannt. Im Alter von zwei Jahren und zehn Monaten dann klinisch auffällige Visusminderung einseitig rechts ohne Schielstellung. Auffällige Weißfärbung der Pupille. Kein Funduseinblick. Differentialdiagnostische Überlegungen (Auflistung nach Unterlagen der beteiligten Augenärzte): congenitale Amotio retinae, zentrales Aderhautkolobom, Papillenanomalie, Retinoblastom, Morbus Coats. Echographisch: Totale Ablatio retinae mit zentraler Trichterbildung.

89. Contents Of  VOLUME 5; NUMBER 2 (OCTOBER) 1998 Incontinentia Pigmenti. (Bloch Sulzberger syndrome) (Bloch Siemen s syndrome). Mohammed Mohy EI-Din Selim ,Tayseer AI-Saad, Mohammed http://www.geocities.com/HotSprings/Spa/8355/vol_6_2.html

Contents of   VOLUME 6; NUMBER 2 (OCTOBER) 1999 Contents Page UVA PHOTOTHERAPY OF ATOPIC DERMATITIS: An experience in Qatar and review of literature. Ahmad Hazem Takiddin, Mohammed Mohy El-Din selim, Hala Mohammed Ezzat Al Homsy, Adel M Kamal An overlap of infantile systemic hyalinosis and Juvenile hyaline fibromatosis: A report of two sisters affected (and review of the literature). Ghalia Al- Thani, Mohammed Mohy El-Din Selim, Hazem Abdulrahman THE PATHOGENESIS OF HYPOPIGMENTED PSORIASIS: Ultrastructural Study of Melanocytes in Psoriatic Lesions . Adel M. Kamal NON VENEREAL TREPONEMATOSES YAWS, BEJEL AND PINTA. Clinical Review and Management . SalimAbdul RahmanAl-Harmozi, Hamda lbrahim Al- Ansari THE TREATMENT OF PERSISTENT AND RECURRENT URETHRITIS IN MALES . M. N. Kamel. EVALUATION OF DIFFERENT METHODS FOR THE TREATMENT OF COMMON WARTS. Abd El Aziz El-Taweel, Ahmed Abd El-Wahab, Adel Kamal, Adel Ali Ali  CAN OPIUM CAUSE CHRONIC ARSENIC POISONING? Simin S. Meymandi, Shahriar Dabiri, Bahram Azadeh

90. DermIS / Main Menu / DOIA / Incontinentia Pigmenti / Images Incontinentia Pigmenti / images http://www.dermis.net/bilddb/diagnose/englisch/i757361.htm

HOME DOIA PeDOIA Skincancer ... DOIA Incontinentia Pigmenti images images for the diagnosis 'Incontinentia Pigmenti' sitesearch: DermIS - Dermatology Information System

91. B From Linkspider UK Health Directory Match », All words -Any word -Exact text. Search », , http://linkspider.co.uk/Health/ConditionsandDiseases/B/

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92. Medicentro 2000;4(3) http://capiro.vcl.sld.cu/medicentro/V4n300/incontinencia.htm

93. Title The summary for this Arabic page contains characters that cannot be correctly displayed in this language/character set. http://www.emro.who.int/umd/ViewWordoftheday.asp?Code=EMT-S004743

94. Specialised UMD Dictionaries The summary for this Arabic page contains characters that cannot be correctly displayed in this language/character set. http://www.emro.who.int/umd/browsingsubj.asp?PageNo=12&subj=311

95. –¢nŽ™–Ô–ŒÇiretinopathy Of PrematurityAROPj The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set. http://svrex.adin.co.jp/home/imis/head_and_neck/eye/retina/ROP.html

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96. New Page 1 Directory Results for B assoicated to Health from Linkspider.org. Keyword Search B assoicated to Health. Search and Browse Information http://www.linkspider.org/index.cgi/Health/ConditionsandDiseases/B/

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