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
Extractions: 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.
Extractions: 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. 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).
Extractions: 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. 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.
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
Extractions: 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.
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
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
Extractions: 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.
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
Extractions: 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.
Extractions: 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.
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
