Entrez PubMed Treatment of shwachman syndrome by Japanese herbal medicine (Juzentaiho-to)stimulatory effects of its fatty acids on hemopoiesis in patients. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
The Pediatric Infectious Disease Journal - UserLogin shwachman syndrome exocrine pancreatic dysfunction and variable phenotypic shwachman syndrome phenotypic manifestations of sibling sets and isolated http://www.pidj.com/pt/re/pidj/fulltext.00006454-200502000-00018.htm
Journal Of Pediatric Hematology Oncology - UserLogin Haematological abnormalities in ShwachmanDiamond syndrome. Isochromosome (7)(q10)in shwachman syndrome without MDS/AML and role of chromosome 7 http://www.jpho-online.com/pt/re/jpho/fulltext.00043426-200306000-00018.htm
Journal Of Pediatric Gastroenterology And Nutrition - UserLogin ShwachmanDiamond syndrome (SDS) a rare autosomal recessive disorder described Shuwachman syndrome shwachman syndrome phenotypic manifestations of http://www.jpgn.org/pt/re/jpgn/fulltext.00005176-200507000-00021.htm
Medical Public Affairs- Press Release People with shwachman syndrome often suffer from undernutrition because the Estimates of how many children have shwachman syndrome vary greatly, http://mednewsarchive.wustl.edu/medadmin/PAnews.nsf/0/39522DBAF92F491B86256B2000
Extractions: SCHOOL HOSTS FIRST INTERNATIONAL CONFERENCE ON RARE CHILDHOOD DISEASE St. Louis, Aug. 5, 1997 Al and Jenny Jenuwine of Allenton, Mich., will be traveling to St. Louis with their 3- and 4-year-old daughters to attend the first international conference on Shwachman Syndrome, a rare genetic disorder that causes malnutrition and a range of other physical problems in children. Emily and Kelsey Jenuwine are severely affected by the disease. The conference will be held at Washington University School of Medicine from 8 a.m. to 4 p.m. Aug. 8 and 9 in the Eric P. Newman Education Center, 320 S. Euclid Ave. The School of Medicine's Division of Pediatric Gastroenterology and St. Louis-based Shwachman Syndrome Support International are co-sponsoring the conference, which is open to health professionals and Shwachman patients and their families. Physicians and families from six countries, including Australia, will attend, and several prominent researchers will offer presentations. "I look at this conference as a first chance for physicians and families to get together to learn more about this unusual problem," said Robert J. Rothbaum, M.D., associate professor of pediatrics and the conference's program director.
Genetic Support Groups,alphabetical List S shwachman syndrome Support Group..http//open.entry.com/medical/shwach.html.shwachman syndrome Support International..http//www.xmission.com/~4sskids http://aspin.asu.edu/geneinfo/sg-s.htm
Extractions: Schizencephaly (Schiz Kids) Listserv http://www.geocities.com/heartland/meadows/7384 Scleroderma Federation http://www.sclerofed.org Scleroderma From A to Z http://www.sclero.org Scleroderma Foundation http://www.scleroderma.org Scleroderma Information Exchange http://hshinc@yahoo.com Scleroderma Resource Foundation http://www.srfcure.org Septo-Optic-Dysplasia Support Group http://members.tripod.com/~roses8 SHARE http://www.nationalshareoffice.com Share and Care Cockayne Syndrome Network http://www.kimbanet.com/~cockayne Short Stature Foundation
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Types Of SCN - Neutropenia Support Association Inc. Severe Neutropenia also occurs in Shwachman s syndrome (Neutropenia Some patientswith shwachman syndrome have developed severe aplastic anemia and http://www.neutropenia.ca/about/types_of_neutropenia.html
Extractions: What is Neutropenia Types of Neutropenia Autoimmune Leukopenia Classic Neutropenia Syndromes Chemotherapy and Neutropenia Patient Evaluation and Treatment ... FAQ Information provide below by: E.L. Sievers, D.C. Dale Audrey Anna Bolyard, R.N., B.S., Tammy Cottle, Carole Edards, R.G.N./R.S.C.N. Bsc., Sally Kinsey, M.D., Beate Schwinzer, Ph.D., Cornelia Zeidler, M.D. Severe chronic neutropenia can exist from birth (congenital neutropenia) or cn occur an any time through life (acquired neutropenia). It may develop by itself or as an accompanying symptom of a different underlying disease. The following list gives you examples of the different types of chronic neutropenias. Metabolic diseases associated with neutropenia Neutropenias that are acquired during life Introduction To meet normal physiologic needs, a healthy adult produces roughly 60 billion neutrophils each day. While neutrophils are produced by the bone marrow at a prodigious rate, their blood half-life is short - on the order of approximately 8 hours in a normal individual. Hence, erythrocytes, with a far longer lifespan, vastly outnumber neutrophils by a ratio of about one thousand to one in the peripheral blood. Under normal physiologic conditions, as stable equilibrium exists between marrow neutrophil production and peripheral utilization. When the production of neutrophils by the bone marrow is outspaced by utilization in the periphery, the number of circulating neutrophils in the peripheral blood decreases and Neutropenia results.
Extractions: PEDIATRICS Vol. 114 No. 3 September 2004, pp. e387-e391 (doi:10.1542/peds.2003-0651-F) This Article Abstract Full Text (PDF) P ... Citation Map Services E-mail this article 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 Kuijpers, T. W. Articles by Hennekam, R. C. M. Related Collections Taco W. Kuijpers, MD, PhD Eline Nannenberg, MD Marielle Alders, MSc Robbert Bredius, MD, PhD and Raoul C. M. Hennekam, MD, PhD
Extractions: This Article Alert me when this article is cited 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 ... [Order Reprint] PubMed PubMed Citation Articles by Harper, K. Articles by Sawyer, W. KJ Harper and WT Sawyer The malabsorption of drugs from the gastrointestinal tract in patients with pancreatic insufficiency is not well documented in the literature. We describe a case of flucytosine malabsorption in a pediatric patient with Shwachman syndrome, a rare disease in the pediatric age group characterized by pancreatic insufficiency. A significant increase in serum concentrations of flucytosine was noted when the drug was administered in a lipophilic vehicle, possibly due to enhanced absorption.
PHP : Resource Details shwachman syndrome Support Services c/o Joan Mowery We facilitate communicationabout shwachman syndrome By * Linking families through exchange of http://www.php.com/include/agency/agency_item.php?AgencyID=1644&where_keywords=
260400 SHWACHMAN-DIAMOND SYNDROME; SDS ShwachmanDiamond syndrome is characterized primarily by exocrine pancreatic (1999) collected data from 116 families with shwachman syndrome. http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:260400] -e
Netwd Health Directory: Shwachman Syndrome Information and resources from Netwd health directory shwachman syndrome. http://netwd.com/diseases/genetic-disorders/shwachman-syndrome.html
The Occurrence Of Leukemia In Patients With The Shwachman Syndrome The occurrence of leukemia in patients with the shwachman syndrome. Woods WG,Roloff JS, Lukens JN, et al. Abstract. No abstract presently available. http://www.meb.uni-bonn.de/cgi-bin/mycite?ExtRef=MEDL/81266588
P53 Protein Overexpression In Shwachman-Diamond Syndrome ShwachmanDiamond syndrome meets many of these criteria2 it is a stem cell disorder shwachman syndrome exocrine pancreatic dysfunction and variable http://arpa.allenpress.com/arpaonline/?request=get-document&doi=10.1043/1543-216
New Medicine 1/2003 Vol. 6 [Asphyxiating Thoracic Dysplasia] shwachman syndrome may present at birth with respiratory distress and thorax . Long bones in shwachman syndrome may show some metaphyseal cupping, http://www.borgis.pl/czytelnia/new_med/2003/01/06.php
Extractions: We describe two children with aspyhyxiating thoracic dysplasia, both whom showed classical radiographic features. The first patient had an asymptomatic clinical course. The second child died soon after the birth. Radiographic appearances of asphyxiating thoracis dystrophy show little variability whereas the clinical course is very versatile. Key words: thoracic dysplasia Introduction Asphyxiating Thoracic Dysplasia (ATD) is a relatively common bone dysplasia occurring in about 1:100.000130.000 births. The major distinctive clinical features are long, narrow thorax, short extremities, short hand, progressive renal disease and hepatic fibrosis (4,5). The major characteristic radiographic findings consist of small thorax, triradiate acetabulum, short tabular bones, and short middle and distal phalanges with cone shaped epiphyses (4, 5). We report two patients ATD, one asymptomatic and one with severe, clinical course and fatal outcome.
