61. List Of Neurological Disorders - Acapedia - Free Knowledge, For blochsulzberger syndrome; Brachial plexus injury; Brain abscess; Brainaneurysm; Brain injury; Brain tumor; Spinal tumor; Brown-Sequard syndrome. http://acapedia.org/aca/List_of_neurological_disorders

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62. GASNet Anesthesiology: Bloch - Sulzberger Syndrome Bloch Sulzberger syndrome - symptoms and caveats http://gasnet.med.yale.edu/pediatric-syndromes/bloch-sulzberger.php

63. Marion Baldur Sulzberger (www.whonamedit.com) Associated eponyms blochsulzberger pigment dermatosis A complex congenital disturbance Sulzberger-Garbesyndrome A syndrome of chronic exudative discoid and http://www.whonamedit.com/doctor.cfm/1660.html

Home List categories Eponyms A-Z Biographies by country ... Contact Marion Baldur Sulzberger American dermatologist, born March 12, 1895, New York City; died November 23, 1983. Associated eponyms: Bloch-Sulzberger pigment dermatosis (Bruno Bloch) A complex congenital disturbance characterized by bizarre, widespread pigmented macules of unusual shapes and defects of teeth, eyes, nails, central nervous system and hair. Sulzberger-Garbe syndrome A syndrome of chronic exudative discoid and lichenoid dermatitis and a severe, nocturnal pruritus. Biography: Marion Baldur Sulzberger was the son of Ferdinand Sulzberger, the owner of one of the largest international meat packing firms in the world. Marion's mother was Stella, his father's third wife. He was a brilliant scholar during his school years, but in his teens he indulged in a rather uninhibited lifestyle, before travelling the world, working as a kitchen hand in Switzerland, a docker in England and a shepherd in Australia. His father died while he was overseas. During World War I Sulzberger was an aviator and eventually achieved the rank of flying instructor. he began his medical studies in Geneva, Switzerland, in 1920, but later changed to the University of Zurich. During this period he came into contact with Josef Jadassohn (1863-1936), professor of dermatology in Bern, and Bruno Bloch (1878-1933), who had been appointed to the chair of dermatology at Zurich in 1916.

64. 1Up Health > Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease) Inform Search 1Up Health. Diseases Conditions . Incontinentia pigmenti syndromeInformation. Guide. Alternative names blochsulzberger's disease. Definition http://www.1uphealth.com/health/incontinentia_pigmenti_syndrome.html

1Up Health Alternative Medicine Clinical Trials Health News ... Health Topics A-Z Search 1Up Health Incontinentia pigmenti syndrome Information Guide Alternative names : Bloch-Sulzberger's disease Definition : An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Jump to a Section of this Guide Definition Causes, Incidence, and Risk Factors Symptoms Prevention ... Calling your Health Care Provider Related Tools and Utilities Search Books on Amazon: Read Articles on eLibrary: Health Products on drugstore.com: Cataract Mental retardation Strabismus More More Topics Central nervous system Genetic counseling and prenatal diagnosis Genetics Hair loss ... More Search 1Up Health A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is the first of its kind, requiring compliance with 53 standards of quality and accountability, verified by independent audit. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s editorial reviewers . A.D.A.M. is also a founding member of Hi-Ethics (www.hiethics.com) and subscribes to the principles of the Health on the Net Foundation (www.hon.ch). Home Contact Us Privacy Links Directory

65. 1Up Health > Incontinentia Pigmenti Syndrome > Causes, Incidence, And Risk Facto Alternative names blochsulzberger's disease. Definition Incontinentiapigmenti syndrome (IPS) is inherited as a dominant X-linked trait. http://www.1uphealth.com/health/incontinentia_pigmenti_syndrome_info.html

1Up Health Incontinentia pigmenti syndrome Alternative Medicine Clinical Trials ... Health Topics A-Z Search 1Up Health Incontinentia pigmenti syndrome Information Incontinentia pigmenti syndrome Causes, Incidence, and Risk Factors Alternative names : Bloch-Sulzberger's disease Definition : An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Causes, Incidence, and Risk Factors 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

66. B Blepharoptosis. Blepharospasm. Blister. blochsulzberger/Siemens syndrome ( Incontinentia Pigmenti). Blood Coagulation Disorders. Blood Platelet Disorders. http://www.mashhadkit.com/iranmedicine/diseases-list/diseases-b.htm

B Babesiosis Back Pain Bacteremia Baker's Cyst ... Bronchiolitis Obliterans Organizing Pneumonia (BOOP) Bronchitis Bronchopulmonary Dysplasia Brown (Tendon Sheath) Syndrome Brown-Sequard Syndrome ... Buruli Ulcer

67. Health Ency.: Disease: Incontinentia Pigmenti Syndrome Ency. home Disease I Incontinentia pigmenti syndrome. Incontinentia pigmentisyndrome See images. Alternative names blochsulzberger's disease. Definition http://www.accessatlanta.com/shared/health/adam/ency/article/001583.html

SEARCH: The Web Yellow Pages HOME AJC.COM 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, hair loss , and central nervous system (CNS) abnormalities. CNS problems may include retardation and delayed development

68. Health Ency.: Index Page dysfunctional uterine Bleeding disorders Bleeding esophageal varices BlepharitisBlepharospasm Blind loop syndrome blochsulzberger's Blocked nasolacrimal duct http://www.accessatlanta.com/shared/health/adam/ency/index/diseidxb.html

SEARCH: The Web Yellow Pages HOME AJC.COM Illustrated Health Encyclopedia Important notice Ency. home Disease Search for a health topic: Find topics alphabetically: A B C D E F ... Z - B - B-cell lymphoma Bacillary angiomatotis (similar to CSD) Back pain - nonspecific Bacteremia with sepsis ... Byssinosis - work-aggravated asthma Please read this Important notice Also Check Out Subscribe to The Atlanta Journal-Constitution Home Autos Classifieds ... Our Sponsors By using AccessAtlanta.com you accept the terms of our Visitor Agreement . Please read it. Privacy statement Registered site users: edit your profile

69. Incontinentia Pigmenti Syndrome blochsulzberger's disease. Causes, incidence, and risk factors Incontinentiapigmenti syndrome (IPS) is inherited as a dominant X-linked trait. http://www.pennhealth.com/ency/article/001583.htm

Disease Injury Nutrition Poison ... Prevention Incontinentia pigmenti syndrome Definition: An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Alternative Names: Bloch-Sulzberger's disease Causes, incidence, and risk factors: 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, hair loss , and central nervous system (CNS) abnormalities. CNS problems may include retardation and delayed development, seizures spasticity , and paralysis Visual problems may develop in up to a third of affected people.

70. Disease Reference dysfunctional uterine Bleeding disorders Bleeding esophageal varices BlepharitisBlepharospasm Blind loop syndrome blochsulzberger's disease Blocked http://www.pennhealth.com/ency/index/diseidxb.htm

Disease Reference A B C D ... Byssinosis - work-aggravated asthma

71. 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

72. 973 12. Kunze S, Frenzel UH, Huttig E, Grosse FR, et al. Klinefelter's syndrome andincontinentia pigmenti blochsulzberger. Hum Genet 1977; 35 237-240. 13. http://www.ato.org.tr/konuk/tdp/tjod/1997-02/973.html

Year:1997 No:3-4 Vol:7 A Turkish case of incontinentia pigmenti with sister chromatin exchange Sevim BALCI1 MD, Ateþ KARA1 MD, Aytaç G?K?Z2 MD, Gülþen K?SE3 MD, Dilek AKTAþ1 MD Genetic Unit Departments of Pediatrics1 and Pathology2, Hacettepe University Faculty of Medicine, SSK Hospital1, Ankara ?ZET Sister kromatin excange çalýþmasý yapýlmýþ bir Türk inkontinansiya pigmenti olgusu Nadir genodermatoslardan olan inkontinansýya pigmenti, erken süt çocukluðundan itibaren özel kutanöz cilt bulgularý ile karakterizedir ve X'e baðlý kalýtým gösterir. Biz yazýmýzda klinik, radyolojik, histopatolojik, sitogenetik ve sister kromatin exchange çalýþmalarý yapýlmýþ olan yeni bir Türk olguyu sunmak istedik. Anahtar kelimeler Ýnkontinansýya pigmenti, sister kromatin exchange, malignancy SUMMARY Incontinentia pigmenti (IP) is a rare genodermatosis, characterised by distinctive cutaneous lesion in early infancy and X-linked inheritance. A new Turkish case of IP with clinical, radiological, histopathological, cytogenetic and sister chromatin exchange findings is reported. Key words Incontinentia pigmenti, sister chromatin exchange, malignancy

73. Search 2 Uff blochsulzberger DISEASE, RN1480, 757.33, *308300. BLOOD COAGULATION CONGENITALDISORDERS, RDG020, 286, D68.9, BLOOM syndrome, RN0830, 757.3, 757.39, Q82.8,210900. http://malattierare.pediatria.unipd.it/cerca_ing/cerca_2_uff.asp?parola=b

74. Iconographie Commentée Translate this page BESNIER-BOECK-SCHAUMANN. BILHARZIOSES (ou schistosomiases). BLÉPHAROCHALASIS. bloch-sulzberger.BLOOM (syndrome de). 1, BLUE RUBBER BLEB NÆVUS. BORST - JADASSOHN. http://www.uvp5.univ-paris5.fr/UV_MED/MINT/DERM/IcoB.HTM

Iconographie commentée Retour images BACTÉRIDES PUSTULEUSES D ANDREWS BAKER-ROSENBACH BALANITE ÉROSIVE ET CIRCINÉE BALANITES ET BALANOPOSTHITES ... Retour

75. Incontinentia Pigmenti : Sites Et Documents Francophones ; naevus chromatophore hereditaire ; syndrome bloch sulzberger . http://www.chu-rouen.fr/ssf/pathol/incontinentiapigmentia.html

Incontinentia Pigmenti Menu général CISMeF Synonyme(s) bloch sulzberger, syndrome ; dermatose pigmentaire eclaboussures ; naevus chromatophore hereditaire ; 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 IPF - association Incontinentia Pigmenti France [Site éditeur Orphanet mots clés : France incontinentia pigmenti type(s) : association patients 20 janvier 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

76. DEUTSCH-SPRACHIGE OPHTHALMOPATHOLOGEN (DOP): Originalbeiträge 1999 in incontinentia pigmenti (Bloch - Sulzberger syndrome). http://www.dog.org/dop/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.

77. Portal.htm Translate this page Retinal signs in the Bloch Sulzberger syndrome. José Luis Guerrero Naranjo, MD,Javier Ortiz Palma, MD, Hugo Quiroz Mercado, MD,. ECOGRAPHIC ICONOGRAPHY. http://www.smo.org.mx/smo/3000_rv73_n4.asp

78. ILDS: ICD-10 - By Code [Q80809 - Q82801] Q823 syndrome Bloch Sulzberger, Q823 Incontinentia pigmenti, Q823 Bloch Sulzbergersyndrome, Q82400 Hypotrichosis in anhidrotic ectodermal dysplasia, http://www.ilds.org/icd10/bycode/Q-02.html

Application to Dermatology of ICD-10 Alphabetized by ICD Code starting with Q: Return to Alphabetical listing... ICD Code: Disorder Ichthyosis vera Alligator skin Ichthyosis congenita (NOS) Keratosis congenita (NOS) Disease Koebner's Koebner's disease Epidermolysis bullosa simple generalised Epidermolysis bullosa simple Koebner Epidermolysis bullosa simple Gedde Dahl Epidermolysis bullosa simple Cockayne Epidermolysis bullosa simple of hands and feet Syndrome Weber Cockayne Weber Cockayne syndrome Ogna variant of epidermolysis bullosa simplex Epidermolysis bullosa simple Ogna Syndrome Herlitz Herlitz syndrome Epidermolysis bullosa Herlitz Epidermolysis bullosa lethal junctional Epidermolysis bullosa recessive generalised dystrophic Epidermolysis bullosa recessive inverse dystrophic Epidermolysis bullosa recessive non-mutilating dystrophic Epidermolysis bullosa recessive localised dystrophic Syndrome Cockayne Touraine Epidermolysis bullosa dystrophic cockayne touraine Cockayne Touraine syndrome Dominant dystrophic epidermolysis bullosa Epidermolysis bullosa albopapuloid Hallopeau Siemens syndrome Syndrome Hallopeau Siemens Herpetiform epidermolysis bullosa Epidermolysis bullosa Dowling Meara Epidermolysis bullosa simple herpetiform Epidermolysis bullosa Pasini Epidermolysis bullosa non-lethal junctional generalised Epidermolysis bullosa non-lethal junctional inverse Epidermolysis bullosa non-lethal junctional localised Disease Goldscheider's Epidermolysis bullosa progressive junctional

79. ILDS: ICD-10 - By Disorder [Bürger Grutz Syndrome - Buschke's Scleredema] P83802 Blister sucking, L03002 Blistering distal dactylitis, Q823 BlochSulzberger syndrome, Q82831 Bloom's syndrome, D22904 Blue cellular nevus, http://www.ilds.org/icd10/bydisorder/B.html

Application to Dermatology of ICD-10 Alphabetized by Disorder starting with B: Return to Alphabetical listing... ICD Code: Disorder Bürger Grutz syndrome B cell lymphoma (NOS) B K mole syndrome Böök syndrome Babesiosis Bacillary angiomatosis in HIV disease Bacterial folliculitis Bacterial skin sepsis (NOS) Bacterid pustular Baghdad boil Bahia ulcer Baker's cyst Balanitis (NOS) Balanitis candidal Balanitis circinata erosiva Balanitis circinate Balanitis irritant Balanitis plasma cell Balanitis xerotica obliterans Balanitis Zoon's Balanoposthitis Baldness (NOS) Baldness male pattern Balloon cell nevus Bamboo hair Bancroftian filariasis Bannayan syndrome Baraitser syndrome Barber's hair sinus Barber's itch Barcoo rot Bardet Biedl syndrome Barium granuloma Barlow's disease Barmah forest virus infection Barraquer Simons disease Bart Pumphrey syndrome Bartholin gland abscess Bartholin Patau syndrome (NOS) Bartholin's cyst Bartholinitis Bartonellosis (NOS) Basal cell carcinoma (NOS) Basal cell carcinoma adenoid Basal cell carcinoma cystic Basal cell carcinoma in HIV disease Basal cell carcinoma metatypical Basal cell carcinoma morphea-like Basal cell carcinoma pigmented Basal cell carcinoma superficial Basal cell carcinoma with follicular atrophoderma Basal cell nevus syndrome Basal cell nevus with comedones Basan syndrome Basidiobolomycosis Basisquamous cell carcinoma Bason's ectodermal dysplasia Bat ear Bath itch Bathing trunk nevus Battered baby syndrome Bayonet hair Bazex syndrome

80. Mioti: Medical Condition Bloch Siemens, • Bloch Sulzberger. • Blood Disorders, • Bloomsyndrome. • Blue Diaper syndrome, • Blue Rubber Bleb Nevus syndrome. http://www.mioti.com/cat/condition/results.asp?Alpha=B

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