Bloch-Sulzberger Syndrome blochsulzberger syndrome, the synonyms, a summary and major features. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome067.html
Extractions: Syndrome Bloch-Sulzberger syndrome Synonyms Asboe-Hansen disease Bloch-Siemens syndrome Bloch-Sulzberger melanoblastoma Siemens-Bloch pigmented dermatosis incontinentia pigmenti (IP) incontinentia pigmenti 1 melanoblastosis cutis linearis sive systematisata melanosis corii degenerativa nevus pigmentosus systematicus Summary A skin pigmentation disorder with malformations of the eyes, teeth, bones, nails, heart, central nervous system, and hair. Mental deficiency is usually associated. The syndrome is divided into two forms: Incontinentia pigmenti type I and type II which lethal in males. Major Features Head and neck: Microcephaly. Eyes: Ocular abnormalities are present in about one-third of all cases. They include strabismus, cataracts, optic atrophy, retrolental fibroplasia, pseudoglioma, retinal detachment, myopia, blue sclerae, nystagmus, microphthalmos, retinal telangiectasia, ophthalmia, and pigmentation disorders of the conjunctiva, iris, retina, and oculomotor paralysis. Thorax: Supernumerary ribs, unilateral breast aplasia, and supernumerary nipples.
Bloch-Sulzberger Syndrome blochsulzberger syndrome, the synonyms, a summary and major features. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
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Incontinentia Pigmenti (Bloch-Sulzberger Syndrome) Incontinentia pigmenti (blochsulzberger syndrome) This disease is described in an article in GeneReviews. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Incontinentia Pigmenti Information Page National Institute Of You are here Home Disorders Incontinentia Pigmenti. NINDS Incontinentia Pigmenti Information Page Synonym(s) blochsulzberger syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Incontinentia Pigmenti (Bloch-Sulzberger Syndrome) Developmental and genetic diseases. Google OMIM PubMed. Incontinentia pigmenti (blochsulzberger syndrome) 46 images from 1 to 15 1 http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Pediatric Neurology Last Updated: February 8, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: Bloch-Sulzberger syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Celia H Chang, MD , Assistant Professor, Department of Neurology, University of California at Davis Celia H Chang, MD, is a member of the following medical societies: American Academy of Neurology , and Child Neurology Society Editor(s): David Griesemer, MD , Chairman of Neurology, Associate Professor, Departments of Pediatrics and Neurology, Medical University of South Carolina; Francisco Talavera, PharmD, PhD , Senior Pharmacy Editor, eMedicine; Kenneth J Mack, MD, PhD , Senior Associate Consultant, Department of Child and Adolescent Neurology, Mayo Clinic; Matthew J Baker, MD
Webkatalog 5. National Library of Medicine bloch-sulzberger syndrome, the synonyms, a summary and major features. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Dermatology Pediatric Diseases Last Updated: April 5, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: IP, Bloch-Sulzberger syndrome, Bloch-Siemens syndrome, familial incontinentia pigmenti, IP2 AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Takuo Tsuji, MD , Chairman, Professor, Department of Dermatology, Nagoya City University, Japan Editor(s): Bernice R Krafchik, MB, ChB , Head, Section of Dermatology, University of Toronto; Professor, Department of Pediatrics, Hospital for Sick Children, Canada; David F Butler, MD Robert A Schwartz, MD, MPH , Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School; Joel M Gelfand, MD, MSCE
Extractions: Medicina (Kaunas) 2005; 41 (6): 496-499 Incontinentia pigmenti (Bloch-Sulzberger syndrome) in neonates Clinic of Neonatology, Faculty of Medicine, Clinic of Skin and Venereal Diseases, Kaunas University of Medicine, Lithuania Key words: incontinentia pigmenti, female, neonatal period, skin alterations, eosinophilia. Summary. A female newborn presented with emerging skin lesions, systemic eosinophilia, and eosinophilic reaction in the skin, liver, lungs, spleen, lymphatic nodes, porencephalia, convulsions, and disorders of thermoregulation. In addition to that, respiratory and heart failure, as well as brain edema were progressing. The suspected diagnosis of incontinentia pigmenti (Bloch-Sulzberger syndrome) was confirmed postmortem by skin biopsy. Received 24 February 2005, accepted 10 May 2005
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Spallone, A. British Journal of Ophthalmology, 1987, Vol 71, 629-634 A Spallone St Gerardo Hospital, Department of Ophthalmology, Monza, Milan, Italy. Seven members from a large family who showed signs of incontinentia pigmenti were examined. A clear X-linked dominant transmission was demonstrated, lethal in males. Study of this family shows that vascular abnormalities of the retina and disorders of the retinal pigment epithelium are the most important ocular lesions in the Bloch- Sulzberger syndrome.
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Jain, R. B. Articles by Willetts, G. S. British Journal of Ophthalmology, 1978, Vol 62, 622-626 RB Jain and GS Willetts
Karger Publishers Incontinentia pigmenti (BlochSulzberger-Syndrome) Case Report and BackgroundIncontinentia pigmenti (IP; bloch-sulzberger syndrome) is an inherited http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowAbstract&ProduktNr=
Extractions: 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. A complex congenital disturbance that occurs almost exclusively in newborn girls (95 %), characterized by bizarre, widespread pigmented macules of unusual shapes; and defects of teeth, eyes, nails, central nervous system and hair. Long lists of other symptoms includes retarded growth and mental retardation. Inheritance is X-linked dominant. It is usually lethal in males, who are probably the result of spontaneous mutations.
