81. Health Library - Thrombocytopenia Absent Radius Founded 1981.Information, networking and support for families children with thrombocytopeniaabsent radius syndrome (tar) syndrome (a shortening of the arms http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29t

82. Shaken Baby Syndrome Truth Foundation TCP can travel with other congenital conditions, such as TCP with Absent Radii (tar)syndrome, May Hegglin syndrome, WiskottAldrich syndrome, and Autosomal http://www.sbstruth.com/Bruising.htm

Shaken Baby Syndrome Shaken Baby Syndrome For Beginners Definition History About Shaken Baby Subdurals ... Bruising and Bleeding Anatomy 101 Motion 101 SBS For Experts Short Falls in Medicine Life of a Subdural Hematoma Biomechanics of Childhood Head Injuries Timing and Dating Childhood Head Injuries ... Bibliography Decide for Yourself SBS 101-For Prosecutors SBS 101- For Defense SBS Diagnosis or Myth? Controversial Questions ... Controversies Detailed Case Studies Case Studies Add a Case Case Analysis Costs Analysis SBS Statistics SBSTruth.com Mission Contact Us Resources Home Bruising and Blood Disorders Disseminated Intravascular Coagulopathies are a group of disorders that affect clotting or thrombosis. These disorders come in both genetic and acquired forms and are not easily diagnosed. Coagulation Disorders produce increased vascular permeability and a decreased ability to clot after suffering a subdural hematoma. Unfortunately, because most of the clotting and complement disorders can only be tested on circulating blood, it is nearly impossible to determine retrospectively, during autopsy, whether a child had a clotting disorder that exacerbated or caused a subdural hematoma. A. Thrombocytopenia (TCP) is a coagulopathy defined by platelet counts less than 100,000/mm of blood. Platelet counts of less than 50,000 have been associated with bleeds from minor trauma whereas platelet counts between 10,000-15,000 results in spontaneous hemorrhages. TCP can travel with other congenital conditions, such as TCP with Absent Radii (TAR) syndrome, May Hegglin Syndrome, Wiskott-Aldrich Syndrome, and Autosomal Recessive TCP. TCP can also be idiopathic. Ideopathic or immune TCP is caused by an autoimmune process which destroys platelets. It is found in 1 in 10,000 people. Ideopathic TCP is generally diagnosed from bruises or petichae on the body or mucosa sinuses, bleeding gums, epistaxis hematuria, menorrhagia, weight loss, fever, and headache. Treatment includes prednisone or splenectomy. TCP has three major causes:

83. The Thoracic Outlet Syndrome significant neurologicalespecially motor- deficit and in the painful syndrome whichremains a) The transaxillary first rib resection (tar) is the most popular http://www.medschool.lsumc.edu/Nsurgery/TOS.html

The Thoracic Outlet Syndrome Annie S. Dubuisson, MD Department of Neurosurgery, CHU Liege, Belgium (Dr. Dubuisson was a peripheral nerve fellow at LSUMC) Abstract: Thoracic outlet syndrome (TOS) is due to compression/irritation of brachial plexus (BP) elements ("neurogenic TOS") and/or subclavian vessels ("vascular TOS") in their passage from the cervical area toward the axilla. The usual site of entrapment is the interscalenic triangle. TOS is a source of disagreement among clinicians regarding its incidence, diagnostic criteria and optimal treatment. Constitutional factors, like a cervical rib, predispose to the development of TOS. The syndrome often develops during the 3rd or 4th decade, following external factors such as trauma, weight excess, incorrect shoulder posture. The clinical picture can be varied: pain in the cervical region and arm, paresthesias (medial side of arm predilected) aggravated by overhead positions of the arms, hand intrinsic muscle deficit/atrophy, easy fatiguability, paleness, coldness of hand. The clinical examination may be entirely normal or show cervical muscle spasm, tenderness of BP in the supraclavicular area, radial pulse attenuation and occurence of symptoms upon positional maneuvers, sensory or motor deficit. The diagnosis is based upon clinical evaluation and absence of other relevant pathology. Therefore, the cervical spine and distal peripheral nerves are studied by radiological and electrophysiological studies. There is no laboratory test confirming TOS: most of the time, there is no anatomic variation seen radiologically and electrophysiological testing is normal. The scalene muscle block appears a helpful diagnostic tool if used with the other clinical data.

84. Diseases Treated - Pediatric BMT - Duke Comprehensive Cancer Center Thrombocytopenia (AMT); Thrombocytopenia with Absent Radii (tar) syndrome.Bone Marrow Failure Disorders Fanconi Anemia; Congenital http://cancer.duke.edu/PBMT/about/diseases.asp

Diseases Treated Allogeneic and autologous transplants are performed for pediatric patients with the following diseases: Acute Leukemia Acute Lymphoblastic Leukemia (ALL) in remission Infant ALL (MLL or 11q23+) T-cell ALL B-precursor ALL Ph+ ALL (T 9;11) ALL with high risk features in first remission at diagnosis including Acute Non-Lymphocytic Leukemia (ANLL) Acute Myelogenous Leukemia (AML) Secondary AML Acute Undifferentiated Leukemia Stem Cell Leukemia Biphenotypic Leukemia Chronic Leukemia Chronic Myelogenous Leukemia (CML) Juvenile CML (JCML) or CMML Myelodysplastic Syndromes (MDS) MDS Monosomy 7 Monosomy 5 Lymphoma Lymphoblastic Lymphoma Large Cell Lymphoma Mantle Cell Lymphoma Histiocytic Lymphoma Brain Tumors Medulloblastoma Astrocytoma Pineoblastoma Retinoblastoma Glioblastoma Multiforme PNET Rhabdoid Brain Tumors Solid Tumors Neuroblastoma Rhabdomyosarcoma Osteogenic Sarcoma Retinoblastoma PNET Immunodeficiency Syndromes Severe Combined Immunodeficiency Syndrome (SCID) X-Linked SCID ADA Deficiency PNP Deficiency Zap-70 Deficiency Idiopathic SCID CID X-Linked Lymphoproliferative Syndrome Common Variable Immunodeficiency Disease (CVID) Wiskott-Aldrich Syndrome (WAS) Cartiledge-Hair Hypoplasia Reticular Dysgenesis Familial Erythrophagocytic Lymphohistiocytosis (FEL) Histiocytic Syndromes Histiocytoisis LHL FEL White Blood Cell Disorders Leukocyte Adhesion Deficiency (LAD) (LFA-1 Deficiency, CD11/18)

85. Search 2 Uff THROMBASTHENIA, RDG030, 287.1, THROMBOCYTOPENIAABSENT RADIUS (tar) syndrome, RN1690,759.89, Q87.2, *274000. THROMBOTIC MICROANGIOPATHIES, RGG010, 446.6, 446.6, M31.1, http://malattierare.pediatria.unipd.it/cerca_ing/cerca_2_uff.asp?parola=t

86. Support Organisations For Parents, Children & Carers: Raisingkids Help and online resources for parents coping with Tourette's syndrome, TARsyndrome, cancer, leukaemia, Hodgkin's and related diseases, and more. http://www.raisingkids.co.uk/sup/sup_T.asp

SITEMAP Site Search Home 1st Time Here? Free Membership! Help! How Do I... ... About Us Support For Parents (Alphabetical Listings): T TAMBA Special Needs Group Charity No 1076478 The Special Needs Group offers support and information to families, regional meetings, and professional study days. TAR Syndrome Support Group Self-help group offering support and telephone contact with others in a similar situation where possible. Teenage Cancer Trust Charity No 1062559 Focuses on the needs of UK teenagers and young adults with cancer, leukaemia, Hodgkin's and related diseases. Terrence Higgins Trust Lighthouse Charity No 288527, Advice and information on welfare rights legal services, employment and housing, and a Hardship Fund (jointly with Crusaid). Tidy Britain Group Tidy Britain Group is an independent UK national charity aiming to improve the quality of local environments. TOFS Charity No 327735 Support and information on Oesophageal Atresia (failure of the 'gullet' to form a continuous tube) and Tracheooesophageal Fistula (an unnatural communication between the windpipe and gullet).

87. Erlaeuterungen http://holger.stolzmann.bei.t-online.de/erlaeuterungen.html

TAR-Syndrom engl.: TAR syndrome TAR-Syndrom n: Kubez. nach ( engl.) Thrombocytopenia- Absent Radius- Syndrome; syn. Radiusaplasie- Thrombozytopenie- Syndrom: autosomal erbl. Fehlbildungssyndrom; mehr als 100 Fälle bekannt; Sympt.: bilaterale Radiusaplasie* ( Daumen vorhanden), Ulna- u. Humerusfehlbildungen , Thrombopenie* inf. verminderter Megakaryozytenprodution mit starker Blutungsneigung in der Lebensmonaten, leukämoide Reaktionen u. Eosinophilie, kuhmilchunverträglichkeit im kleinkindesalter; fakultativ Fehlbildungen der unteren Extremitäten ( in über 50%) u. angeborene Herzfehler (in ca. 30%). engl. = thrombocytopenia-absent radius syndrome) autosomal-rezessiv erbliche symmetrische Radiusaplasie, kombiniert mit Thrombozytopenie (verminderte Megakaryozytenproduktion) sowie anderen (variablen) Skelettfehlbildungen; häufig Herzfehler. Phokomelie engl.: phocomelia »Robbengliedrigkeit«, durch rudimentäre Entwicklung der langen Röhrenknochen bedingte Defektfehlbildung der Extremitäten mit rel. normal ausgebildeten Händen bzw. Füßen; z.B. bei Thalidomid-Embryopathie, SC-Syndrom. Tetraphokomelie engl.:

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