Entrez-PubMed read Fine mapping of the locus for shwachmanDiamond syndrome at 7q11, identificationof shared disease haplotypes, and exclusion of TPST1 as a candidate gene. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Shwachman-Diamond Syndrome Canada Translate this page Alérion shwachman-Diamond syndrome Canada. PO Box 502 WolfvilleNova Scotia B0P 1X0 Projets actifs à l'Université Laval. http://www.ulaval.ca/vrr/rech/Prog/org010356.html
Shwachman-Diamond Syndrome Canada Translate this page Alérion shwachman-Diamond syndrome Canada. PO Box 502 Wolfville Nova ScotiaB0P 1X0 Programmes de recherche. Projets actifs à l'Université Laval http://www.ulaval.ca/vrr/rech/Proj/org010356.html
Shwachman Diamond Syndrome shwachman Diamond syndrome. shwachman Diamond syndrome is a rare condition that involvesthe pancreas and bone marrow it makes them unable to function normally. http://members.tripod.com/shwachmandiamondkids/
Extractions: Brandon loves his TIVO! Our prayers go out to Jeff, Dani's Fiancé'. He is in the desert now! We are thinking of you Jeff. God Bless the USA!!! Shwachman Diamond Syndrome Shwachman Diamond Syndrome is a rare condition that involves the pancreas and bone marrow it makes them unable to function normally. It is usually diagnosed in infancy or early childhood and is an inherited condition. This condition causes the pancreas to not function properly, therefore they are unable to digest food properly. This leads to the difficulty gaining weight. The Bone Marrow may not produce all of the blood cells in normal number, especially infection fighting white blood cells. These are called Neutrophils. Bone Marrow failure may develop over time. Other things associated with SDS are short stature, skeletal abnormalities, learning difficulties, frequent infections, liver, kidney and dental problems. It is important to know that not all children born with SDS will have all of the symptoms of the disease. Brandon does not have all of the signs and symptoms of SDS. He has many of them. His lifestyle is much different than most 4 year olds. He goes to the doctor once a week for a blood test. He receives injections at home. Has high fevers and infections that hospitalize him. We are watching his Marrow closely so he has a Bone Marrow Biopsy done every 6 Months or so. His Neutrophils are unable to get to the site of infection. (Chemostaxis)
Shwachman Diamond Syndrome shwachman diamond syndrome,, Print this article, shwachman diamond syndrome,Fig. 1 Pelvis and femora of a boy with shwachman Diamond syndome. http://www.amershamhealth.com/medcyclopaedia/Volume VII/SHWACHMAN DIAMOND SYNDR
Extractions: *For Medical Professionals only, registration required Shwachman diamond syndrome, (Harry Shwachman, 20th century, American paediatrician; Louis Diamond, 20th century, American haematologist), (also called metaphyseal chondrodysplasia with exocrine pancreatic insufficiency ), growth retardation, short limb dwarfism, low birth weight, pancreatic insufficiency, malabsorption, recurrent infection and neutropenia. Radiologically, there is mild metaphyseal dysplasia with irregularity of the metaphyses close to the zone of provisional calcification ( Fig.1 ). The pancreas may be shown to be fatty on either MRI or ultrasound.
The Hospital For Sick Children - Release FOR IMMEDIATE RELEASE December 23, 2002. Sick Kids researchers identifygene for shwachmanDiamond syndrome. You are here Current HSC News. http://www.sickkids.on.ca/mediaroom/custom/sdsgene.asp
Extractions: You are here Current HSC News TORONTO - Researchers at The Hospital for Sick Children (HSC) and the University of Toronto (U of T) have identified the gene that is altered in Shwachman-Diamond syndrome. The researchers studied 250 Shwachman-Diamond syndrome families from around the world and identified two major disease-causing mutations in a gene on chromosome 7. This research is reported in the January issue of the scientific journal Nature Genetics. Shwachman-Diamond syndrome (SDS) is a relatively rare genetic disorder that occurs in approximately one in 50,000 births. SDS affects many organs in the body. Primary features of SDS include a defect in the pancreas that leads to difficulties in digesting food, hematologic (blood) problems with inadequate production of some types of white blood cells, skeletal abnormalities, and short stature. The hematologic problems make people with SDS prone to severe, sometimes fatal infections, and some die from blood complications such as leukemia or bone marrow failure.
Extractions: Date Prev Date Next Thread Prev Thread Next ... Thread Index 15 FEB 01 The Office of Research Services (ORS) has recently obtained the following information which we are forwarding to list members. ******************* Please note that all applications/proposals/letters of intent must be approved by Research Services using an SFU Research Funding Application Signature Sheet prior to their submission. This form can be found on the website at: http://www.css.sfu.ca/sites/ors/AppSheet.html and must accompany a copy of the application for ORS records. Applicants are strongly advised to allow sufficient lead time for the proper consideration at each level. ******************* AGENCY: Shwachman-Diamond Syndrome (SDS)-Canada PROGRAM: Research Grants TYPES: (i) letter of intent; (ii) application DEADLINES: (i) 15 MAR 02; (ii) 15 MAY 01 (by invitation) See: http://www.shwachman.org
Extractions: Thank you to everyone who came out for golf and/or dinner/auction, and special thanks to our sponsors, volunteers, and Deer Creek. 2003 Sponsors included: Art Gallery of Ontario Bowne Burger King Casa Loma Famous Player's NHLPA Roots Royal Ontario Museum Second City Sports Clubs of Canada Toronto Symphony Orchestra Be sure to keep up on the Alumnae events; there's something for everyone! And if you missed us this year - never fear ~ we'll be back in May 2003!! 2000 AOII Tournament
IRSC - Rare Disorders ca Through an educational and informational support network, CEDA is committed tothe enhancement of the lives of all persons affected by EhlersDanlos syndrome http://www.irsc.org:8080/irsc/irscmain.nsf/cat?readform&cat=Rare Disorders&type=
Stichting Shwachman Syndroom Support Holland Hoe u in het bezit kan komen van meer informatie en wie zijn de bestuursleden? Feitenvan het syndroom en een aantal bruikbare tests voor een goede diagnose. http://www.shwachman.nl/
Extractions: Hoe u in het bezit kan komen van meer informatie en wie zijn de bestuursleden? Feiten van het syndroom en een aantal bruikbare tests voor een goede diagnose. Links naar andere SSS groepen, en andere relevante onderwerpen. Informatie over onze sponsors en hoe u sponsor kunt worden. Acquisitie stellen wij niet op prijs, sponsoring echter wel. We don't like acquisition, instead we like sponsoring. Dat we zover gekomen zijn hebben we mede te danken aan: 3 maart 2002
Wildpuppy's Home Page 3 Our shwachmanDiamond Children. This is one of the captured pictures takenat the shwachman convention in St.Louis this last August 1997. http://members.aol.com/wildpuppy/shwachman.index.html
Index Of /~sssa Parent Directory 19Jul-20002020 - Apache/1.3.22 Server at home.vicnet.net.au Port 80Index of /~sssa. Name Last modified Size http://home.vicnet.net.au/~sssa/
Pancreatic Elastase-1 Detailed Chronic Pancreatitis, Cystic Fibrosis, Diabetes mellitus, ShwachmanSyndrome and other ailments. EU registration number DE/CA80/7.001. http://www.bioserv-diagnostics.com/gastroenterology/pancreatic_elastase_detailed
Extractions: page up Details on the determination of human fecal pancreatic Elastase-1 with the BIOSERV ELISA For the diagnosis of a pancreatic insufficiency, which may be caused by Chronic Pancreatitis, Cystic Fibrosis, Diabetes mellitus, Shwachman Syndrome and other ailments EU registration number DE/CA80/7.001 Advantages of the BIOSERV ELISA kit for the detecti on of fecal pancreatic elastase-1 in stool Principle of the test S andwich-ELISA with polyclonal antibodies directed against defined sequences of the human pancreatic elastase-1. Sample material: stool Medical indications for the application of the test E xocrine pancreatic insufficiency , caused by C hronic pancreatitis is a progressing disease causing the original and functional pancreatic parenchyma to degenerate in a gradual sclerotic process. Characteristic features are its symptoms (abdominal pain, steatorrhea, loss of weight), typical morphological changes of the
