21. Literatuurdatabase Erfelijkheid alternatieve geneeswijzen, alvleesklier, ambulante zorg, amyloidose,amyoplasia congenita, androgeen ongevoeligheids syndroom, anesthesie, anticonceptie http://www.erfelijkheid.nl/documentatie/index.php?pulldown=amyoplasia congenita

22. Zoek Onderwerpen Op Deze Site Met De Letter A amyoplasia congenita publicaties Amyotrofe lateraal sclerose, ZIE ALS aN-acetylgalactosaminidase deficiëntie - Andermann s Syndroom nieuwsberichten http://www.erfelijkheid.nl/onderwerpen/A.php

A B C D E ... OVERIG Onderwerpen op erfelijkheid.nl met de letter A a-1 antitrypsine deficiëntie, ZIE AAT deficiëntie Aangeboren / erfelijk / nieuwe mutatie Aangezichtsafwijkingen AAT deficiëntie AAT deficiëntie: informatie voor (para)medici ... ADHD: veelgestelde vragen Adipositas, ZIE Obesitas Adrenogenitaal syndroom (AGS) Adrenogenitaal syndroom (AGS): publicaties Adrenoleukodystrofie (ALD) Adrenoleukodystrofie, X-gebonden (X-ALD) ... Albinisme: publicaties Alfa-1 antitrypsine deficiëntie, ZIE AAT deficiëntie Alfa-1,4 Glucosidase Deficiëntie Alfa-Galactosidase A Deficiëntie, ZIE Fabry, ziekte van Alfa-Galactosidase B Deficiëntie Alfa-L-Fucosidase Deficiëntie Alfa-L-Iduronidase Deficiëntie Alfa-N-acetylgalactosaminidase deficiëntie ... Alfa-Neuraminidase deficiëntie Alfa-Thalassemie, ZIE Thalassemie Allgrove, syndroom van: publicaties ALMS, ZIE Alström syndroom Alport, Syndroom van Alport, syndroom van: publicaties ALS (Amyotrofe lateraal sclerose) ALS: nieuwsberichten ... ALS: publicaties ALSS, ZIE Alström syndroom Alström syndroom Alstrom-Hallgren syndroom, ZIE Alström syndroom Alvleesklierkanker: nieuwsberichten Alzheimer, ziekte van

23. SupportPath.com: Arthrogryposis Multiplex Congenita Arthrogryposis Multiplex Congenita. Also called AMC, amyoplasia congenita.Other topics of interest on SupportPath.com Birth Defects, disABILITIES. http://www.supportpath.com/sl_a/arthrogryposis_multiplex_congenita.htm

Arthrogryposis Multiplex Congenita Also called: AMC, Amyoplasia Congenita Other topics of interest on SupportPath.com: Birth Defects disABILITIES About Us Add-A-Link ... here Online Communities / Message Boards... Adults with AMC (amc_adults) Website: http://groups.yahoo.com/group/amc_adults/ Description: "This is a mailing list for adults with arthrogryposis to come together and communicate with others affected with amc." You must register to post to this Yahoo Group Date Added: 07/19/2002 Website: Description: Yahoo Group Date Added: 08/08/2002 Arthrogryposis Support Group (arthrogryposissupportgroup) Website: http://groups.yahoo.com/group/arthrogryposissupportgroup/ Description: This Yahoo Group states: "This group was created for children and adults with amc to communicate with one another." Registration is required to post. Date Added: 07/19/2002 Online Chats... Note: Regularly scheduled chats are listed on our NEW Online Events Calendar Links in this section are primarily to chat rooms open 24/7 which may or may not be moderated. None Listed Usenet Groups...

24. Health Library - Neurogenic Arthrogryposis Multiplex Congenita; Myopathic Arthrogryposis MultiplexCongenita; GuerinStern Syndrome; amyoplasia congenita http://yalenewhavenhealth.org/library/healthguide/en-us/illnessconditions/topic.

25. Penn State Faculty Research Expertise Database (FRED) amyoplasia congenita, Arthromyodysplasia, Congenital. GuerinStern Syndrome,Myodystrophia Fetalis Deformans. Congenital Arthromyodysplasia, Arthrogryposes http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D001176

26. Journal Of Pediatric Orthopaedics - UserLogin A multidisciplinary approach to amyoplasia congenita (classic arthrogryposis).Orthop Trans 1986;10130. Context Link. 27. Sarwark JF, MacEwen GD, http://www.pedorthopaedics.com/pt/re/jpedortho/fulltext.00004694-199601000-00026

LWWOnline LOGIN eALERTS REGISTER ... Archive You are attempting to access protected content. To access this content please login using an established account or create/activate an account. If you have already created/ activated an online account, please login below: User Name: Password: Note: passwords are CASE SENSITIVE If you are a new user or guest visiting an LWWonline site for the first time, please complete the new account setup process to view or purchase content. Forgot your password? Subscribe Renewal Information Subscribe to RSS feed utrdc-pt02 Release 4.0

27. Medline Abstracts, Arthrogryposis, 1997-1998 Arthrogryposis multiplex congenita, craniofacial, and ophthalmological deformity in classical arthrogryposis multiplex congenita (amyoplasia congenita). http://sonnet1.sonnet.com/avenues/research/biblio1b.htm

home networking medical professionals research ... other resources Medline Abstracts, Arthrogryposis, 1997-1998 Pediatr Surg Int Successful separation of thoraco-omphalopagus and ischiopagus tetrapus twins in Korea. Jung PM Pediatric Surgical Division, Department of Surgery, Hanyang, University Hospital, 17 Haengdang dong, Sung dong ku, Seoul, Korea. MeSH Terms: Abnormalities, Multiple/surgery* Adult Case Report Colon/abnormalities* Female Follow-Up Studies Human Ileum/abnormalities* Infant, Newborn Ischium/abnormalities* Male Pregnancy Thorax/abnormalities* Twins, Conjoined/surgery* PMID: 9354737, UI: 98022986 back to list Anaesth Intensive Care 1997 Oct;25(5):546-9 Intraoperative convulsions in a child with arthrogryposis. Ferris PE Department of Anaesthesia, Royal Alexandra Hospital for Children, Westmead, N.S.W. A case of intraoperative convulsions occurring in a child with arthrogryposis multiplex congenita is presented. Arthrogryposis and the anaesthetic management of children with this condition is discussed. Factors which may have contributed to the convulsions are considered. MeSH Terms: Arthrogryposis/physiopathology* Case Report Convulsions/etiology* Fever/etiology Fundoplication Gastroesophageal Reflux/surgery Human Infant Intraoperative Complications* Intubation, Intratracheal

28. Medline Abstracts, Arthrogryposis, 1997-1998 in a fetus associated with arthrogryposis multiplex congenita and amyoplasia in classical arthrogryposis multiplex congenita (amyoplasia congenita) http://sonnet1.sonnet.com/avenues/research/titles1a.htm

home networking medical professionals research ... other resources Medline Abstracts, Arthrogryposis, 1997-1998 Titles: Congenital Rapidly Fatal Form of Nemaline Myopathy with Fetal Hydrops and Arthrogryposis. a case report and review Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24 Large-scale deletions in a Chinese infant associated with a variant form of Werdnig-Hoffmann disease Improved oxygenation following adenosine infusion in persistent pulmonary hypertension of the newborn ... melissa schmidt

29. %108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5 Altman, HS; Davidson, LT amyoplasia congenita (arthrogryposis multiplex congenita).J. Pediat. 15 551557, 1939. 3. Bamshad, M.; Jorde, LB; Carey, http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:108145] -e

30. +121050 CONTRACTURAL ARACHNODACTYLY, CONGENITAL KingsleyPillers, EM Arachnodactyly with amyoplasia congenita. Proc. Roy. Soc.Med. 39 696-697, 1946. 23. Langenskiold, A. Congenital contractural http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:121050] -e

31. Elsevier.com - Smith S Recognizable Patterns Of Human Malformation amyoplasia congenita Disruptive Sequence Distal Arthrogryposis Syndrome, Type 1PenaShokeir Phenotype Cerebro-Oculo-Facio-Skeletal (COFS) Syndrome Lethal http://www.elsevier.com/wps/product/cws_home/705571

Home Site map Regional Sites Advanced Product Search ... Smith's Recognizable Patterns of Human Malformation Book information Product description Audience Author information and services Ordering information Bibliographic and ordering information Book related information Submit your book proposal Other books in same subject area About Elsevier Select your view SMITH'S RECOGNIZABLE PATTERNS OF HUMAN MALFORMATION To order this title, and for more information, go to http://www.elsevierhealth.com/title.cfm?ISBN=0721606156 Sixth Edition By Kenneth Jones , MD, Professor of Pediatrics; Chief, Division of Dysmorphology and Teratology, University of California, San Diego, School of Medicine, La Jolla, CA Description The completely revised and updated New Edition of this definitive text?now in full color! Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides a wealth of information on normal and abnormal morphogenesis * minor anomalies and their relevance * clinical approaches to specific diagnoses * and normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormality?including occasional associated abnormalities?natural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality.

32. EMedicine - Arthrogryposis : Article By Harold Chen, MD, MS, FAAP, FACMG Arthrogryposis Arthrogryposis, or arthrogryposis multiplex congenita, in classical arthrogryposis multiplex congenita (amyoplasia congenita). http://www.emedicine.com/ped/topic142.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Arthrogryposis Last Updated: April 21, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: arthrogryposis multiplex congenita, multiple congenital contractures, multiple congenital joint contractures, fetal akinesia, decreased fetal movements, development of extra connective tissue, fixation of the joint, joint fixation, scoliosis, limb dysfunction, joint deformity, limb malformations AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Harold Chen, MD, MS, FAAP, FACMG , Chief, Professor, Department of Pediatrics, Section of Perinatal Genetics, Louisiana State University Medical Center Harold Chen, MD, MS, FAAP, FACMG, is a member of the following medical societies: American Academy of Pediatrics American College of Medical Genetics American Medical Association American Society of Human Genetics , and Teratology Society Editor(s): James Bowman, MD

33. EMedicine - Neonatal Brachial Plexus Palsies : Article By Jennifer Semel-Concepc amyoplasia congenita (a form of arthrogryposis) can be distinguished from BPP byrigidity of the joint and skin dimpling. http://www.emedicine.com/pmr/topic215.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Physical Medicine and Rehabilitation Plexopathy Neonatal Brachial Plexus Palsies Last Updated: August 3, 2001 Rate this Article Email to a Colleague Synonyms and related keywords: brachial plexus injury, obstetric brachial plexus palsy, obstetrical brachial plexus palsy, brachial plexus palsy, brachial plexus birth palsy, birth brachial plexus palsy, traumatic peripheral nervous system injury, congenital brachial plexus palsy, Erb's palsy, Klumpke's palsy, brachial plexopathy, Duchenne-Erb's palsy AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Jennifer Semel-Concepcion, MD , Medical Director, Assistant Professor, Department of Physical Medicine and Rehabilitation, St. Charles Hospital and Rehabilitation Center Coauthor(s): Anne Conway, PT

34. Treatment Of Pain With Gabapentin In A Neonate -- Behm And Kearns 108 (2): 482 - During this time, the diagnosis was refined to amyoplasia congenita, a sporadicabnormality most likely caused by hypotension in the developing fetal spinal http://pediatrics.aappublications.org/cgi/content/full/108/2/482

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Extract P Rs: Submit a response Alert me when this article is cited ... Alert me if a correction is posted 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 ... Download to citation manager PubMed PubMed Citation Articles by Behm, M. O. Articles by Kearns, G. L. Related Collections PEDIATRICS Vol. 108 No. 2 August 2001, pp. 482-484 EXPERIENCE AND REASON: Treatment of Pain With Gabapentin in a Neonate Gabapentin (GBP) is a gamma-aminobutyric acid (GABA) analog approved for the treatment of partial seizures with and without generalization in patients 12 years of age and older. The precise mechanism of action for GBP in the central nervous system is not known. Although it was originally designed to mimic the effects of GABA, it has been found to be inactive at GABA binding sites. Recently, GBP has been shown to be effective in the treatment of neuropathic pain in adults and children.

35. Arthrogryposis; A Clinical And Pathological Study Of Three Cases -- Kanof Et Al. He was impressed by the clinical and histologic changes in the muscles about theaffected joints, and coined the name amyoplasia congenita. http://pediatrics.aappublications.org/cgi/content/abstract/17/4/532

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Alert me to new issues of the journal Add to My File Cabinet ... Download to citation manager PubMed Articles by Kanof, A. Articles by Volk, B. W. Pediatrics, Apr 1956, 532-540, Vol 17, No. 4 Arthrogryposis; A clinical and pathological study of three cases A Kanof, SM Aronson and BW Volk 80 Linden Boulevard, Brooklyn 26, New York. The term arthrogryposis multiplex congenita is used to describe a syndrome of congenital malformations, the chief of which is flexion deformity of the joints. This name, and multiple congenital articular rigidities, used in the first description of this entity by Rocher did not seem appropriate to Sheldon because they seemed to indicate primary involvement of the joints. He was impressed by the clinical and histologic changes in the muscles about the affected joints, and coined the name amyoplasia congenita.

36. PharmGKB: Arthrogryposis Alternate Names, amyoplasia congenita; Arthrogryposes; Arthromyodysplasia,Congenital; Arthromyodysplasias, Congenital; Congenital Arthromyodysplasia; http://www.pharmgkb.org/do/serve?objId=PA443435&objCls=Disease

37. A&A -- Sign In Page A patient with amyoplasia congenita (1) and previous unsuccessful endotrachealintubation with standard/McCoy laryngoscopy, intubating laryngeal mask, http://www.anesthesia-analgesia.org/cgi/content/full/99/6/1879

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to Full Text MRI of the Upper Airway and McCoy-Balloon Laryngoscopy with Left Molar Approach... Mentzelopoulos et al. Anesth Analg. This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a colleague Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Download to citation manager PubMed PubMed Citation Articles by Mentzelopoulos, S. D. Articles by Kostopanagiotou, G. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 1 day for US$15.00 Regain Access - You can regain access to a recent Pay per Article purchase if your access period has not yet expired.

38. Arthrogryposis Multiplex Congenita (AMC) amyoplasia congenita. congenital arthromyodysplastic syndrome. congenital articularrigidity. congenital contractures of extremities http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome039.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome arthrogryposis multiplex congenita (AMC) Synonyms Guérin-Stern syndrome Otto syndrome Rocher-Sheldon syndrome Rossi syndrome amyoplasia congenita congenital arthromyodysplastic syndrome congenital articular rigidity congenital contractures of extremities multiple congenital articular rigidity multiple congenital contractures myodysplasia fibrosa multiplex myodysplasia foetalis deformans myodystrophia foetalis deformans neuro-arthromyodysplasia pterygium universale pterygo-arthromyodysplasia congenita Summary Major Features Head and neck: Facial asymmetry, micrognathia, immobile facies, notched chin, and malar hypoplasia. Ears: Low-set ears posteriorly angulated ears, and overfolded helices. Eyes: Keratoconus, downslanting palpebral fissures, blepharoptosis, hypertelorism, ophthalmoplegia, and retinopathy. Nose: High nasal bridge. Mouth and oral structures: Highly arched palate, cleft lip, cleft palate, and trismus. Neck: Short neck, fused cervical vertebral, and pterygia.

39. Search Jablonski's Syndromes Database CongenitalMSH/EP/D001176 MTH/MM/U009504 MSH/EN/D001176 http://www.nlm.nih.gov/cgi/jablonski/syndrome_cgi?term=amyoplasia congenita&fiel

40. Index A: Contact A Family - For Families With Disabled Children: Information On amyoplasia congenita see Arthrogryposis Amyotrophic Lateral Sclerosis see MotorNeurone disease Anaphylaxis Andersen disease see Glycogen Storage diseases http://www.cafamily.org.uk/Idx/a.html

printer friendly home how we can help medical information ... how you can help Please use the index below to access the condition you require information on. It may take longer to find what you are looking for this way compared with our "search this site" facility in the navigator on the left but we try to point you in the most appropriate direction using this index and therefore the results should be better. For speed, this index has been split into separate alphabetical files: numbers 0-9 A B C ... Z Contact a Family also has information on many other specific conditions and rare disorders. If you cannot find the information you require in The Contact a Family Directory Online , you may wish to use our Contact a Family Helpline service. aAA see Acquired Aplastic Anaemia ACI see Arterial Calcification of Infancy ADA see Primary Immunodeficiencies ADD see Attention Deficit Hyperactivity Disorder ADEM see Acute Disseminated Encephalomyelitis (ADEM) ADHD see Attention Deficit Hyperactivity Disorder AHO see Albright Hereditary Osteodystrophy AHO with Pseudo Hypoparathryrodism see Albright Hereditary Osteodystrophy AHO with Pseudo Pseudo Hypoparathryrodism see Albright Hereditary Osteodystrophy AHT see Thyroid Disorders AIDS see HIV Infection and AIDS ALA Dehydratase deficiency see

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 2     21-40 of 98    Back | 1  | 2  | 3  | 4  | 5  | Next 20