MUMS List Of Disorders - A Multiplex congenita (19) *; Arthrogryposis Multiplex congenita, AmyoplasiaType (1); Arthrogryposis, Classic (1) *; Arthrogryposis, Distal http://www.netnet.net/mums/mum_a.htm
Extractions: indicates there is a support group which covers that diagnosis. 2 Hydroxic Gluteric Urea (1) 2 Keto Adepic Aciduria (1) 3 Hydroxy 3-Methylglutaryl CoAlyase Deficiency (HMG) (1) * 3 Methycrotonyl CoA Carboxylase Deficiency (3MCCC) (1) 3 Methylglutaconic Aciduria (4) 4 Hydroxybutyric Aciduria (1) 5 Alpha Reductase Deficiency (1) * 5 Oxoprolinuria (Pyroglutamic Aciduria) (1) 18 Hydroxylase Deficiency (Adrenal Hyperplasia) (1) 21 Hydroxylase Deficiency (Adrenal Hyperplasia) (18) ** ACTH Deficiency (1) AIDS (Acquired Immune Deficiency Syndrome) (6) ** Aarskog Syndrome (8) ** Abdominal Chylous Ascites (abdomen fills w/fluid) (4) Abdominal Migraines (2) Abdominal Teratoma Tumor (5) Abetalipoproteinemia (4) * Abetalipoproteinemia (Bassen-Kornzweig Syndrome) (1) * Absence of Arm Below Elbow, Congenital (25) * Absence of Arms (Severed in accident) (2) * Absence of Arms, Hands attached to shoulder (1) * Absence of Extensor Tendons in hands - bilateral (1) * Absence of Feet and Hands, Congenital (2) *
Arthrogryposis Arthrogryposis Group (TAG), United Kingdom (UK), physiotherapy overview (.pdf)Also See Arthrogryposis multiplex congenita, I Alfonso, O Papazian, et. http://www.kumc.edu/gec/support/arthrogr.html
Extractions: Rossin syndrooma Sairauden nimi, AMC, tulee englanninkielisistä sanoista Arthrogryposis Multiplex Congenita. Se tarkoittaa synnynynnäistä monioireista nivelten jäykistymäsairautta, jota kutsutaan myös Amyoplasiaksi. Taudin klassisessa muodossa esiintyy monenlaisia niveljäykistymiä ja epämuodostumia; mm. koukkusormet- ja polvet, kieroutuneet lonkat, sisäänkiertyneet olkapäät sekä virheasennossa olevat jalkaterät. Myös kitalakihalkiot, sydänviat ja muut epämuodostumat ovat yleisiä. Pahimmassa tapauksessa aivotkin ovat epämuodostuneet ja seurauksena on psyykkinen kehitysvammaisuus Tauti voi johtua raskaudenaikaisesta sikiön lihassairaudesta, äidin raskaudenaikaisesta sairaudesta tai sikiön keskushermostovauriosta. AMC-lapsia arvioidaan syntyvän suhteessa 1/3000 kaikista lapsista. Kaikista tapauksista n. 30 %:a arvioidaan perinnöllisiksi Fysioterapeuttisilla ja kirurgisilla hoidoilla voidaan huomattavasti auttaa AMC-vammaisia. Sairaus ei ole etenevä, ja se voi ilmaantua klassista taudinkuvaa lievempänä. Lisätietoja: A National Support Group for Arthrogryposis Multiplex Congenita, USA
Arch Pediatr Adolesc Med -- Page Not Found Arch Pediatr Adolesc Med. 155;407408, March 2001, Picture of the Month, http://archpedi.ama-assn.org/issues/v155n3/ffull/ppm00283-1.html
Extractions: The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"
ELibrary.com - The Mosby Medical Encyclopedia 10-01-1996, eLibrary is the subscription based online library for fun or research. Find out more about securing your guaranteed Free 7day trial with your credit card and retrieve 'eLibrary.com - The Mosby Medical Encyclopedia 10-01-1996, 'arthrogryposis http://redirect-west.inktomi.com/click?u=http://ask.elibrary.com/getdoc.asp%3Fpu
DSHI Systems - Medical Glossary AMPULLA OF VATER; AMPUTATION; AMPUTATIONS; AMYLASE; AMYLOIDOSIS; AMYOPLASIACONGENITA; AMYOTROPHIC LATERAL SCLEROSIS (ALS); ANA; ANA KIT; http://www.mymedadvice.com/html/A_list.htm
Last Updated 15.03.2001 BRCA1 carriers; Aetiological factors in neonatal cholestasis; AmyoplasiaCongenita Picture of the Month; Bone marrow cytogenetic http://www.rusmedserv.com/genetics/review/rev1503.htm
Extractions: A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers Aetiological factors in neonatal cholestasis Amyoplasia Congenita - Picture of the Month Bone marrow cytogenetic abnormalities of aplastic anemia ... Treatment of 193 Episodes of Laryngeal Edema With C1 Inhibitor Concentrate in Patients With Hereditary Angioedema
Society For Pediatric Anesthesia The authors report the successful treatment of pain in an infant with amyoplasiacongenita with severe contractures and dislocated joints. http://www.pedsanesthesia.org/newsletter/2002winter/commentary.shtml
Extractions: Committee on Drugs Pediatrics This document is a statement from the AAP Committee on Drugs regarding unintentional acetaminophen overdosing and subsequent toxicity. There are many liaisons and consultants to the Committee on Drugs listed at the conclusion of he statement, including Dr. Cote, from the AAP Section of Anesthesiology and Pain Treatment. The paper discusses the report that a dose of 120-150 mg/kg as the minimal single acetaminophen dose associated with hepatotoxicity. Fasting is associated with increased acetaminophen toxicity in animal studies and human observations. The clinical presentation of acetaminophen toxicity has been divided into 4 phases. First, anorexia, nausea, vomiting, malaise and lethargy may actually lead to administration of additional acetaminophen. The second phase, the initial signs resolve and right upper quadrant pain and tenderness develop. Bililrubin and liver enzymes become elevated and prothrombin time is prolonged. Three to five days into the course of toxicity the third phase begins, consisting of malaise, vomiting as well as signs of hepatic failure ( hypoglycemia, jaundice, coagulopathy, encephalopathy). the fourth phase is either death or progression to recovery. Treatment with N-acetylcycteine (NAC) should begin with 6-8 hours of acetaminophen and following a dose of activated charcoal. NAC has been given PO but there are investigators using it IV. The statement concludes with recommendations to health care providers which will likely decrease the incidence of acetaminophen toxicity.
