81. Arthrogryposis Multiplex Congenita (AMC) - Homepages Of People Who Have A Disabi Arthrogryposis Multiplex congenita (AMC) This website links together the a rare condition called arthrogryposis (amyoplasia) at first it was hard, http://www.linkable.org/arthrogryposi.html

Personal Pages of People who have Arthrogryposis Multiplex Congenita (AMC) Home What's New Members Home Medical ... Alina Echemendia - My world. AMC Roy - Roy Silvernail"s Page Casey Linn - Provides photographs, family and personal information and favorite links. Casey's Corner - Pictures of me and the love of my life. Cici's Arthrogryposis Page - I was born with arthrogryposis so I'm creating this site for arthrogryposis patients. confoozled.com Dan's Place - Florida male with arthrogryposis shares his interests. Denise's Page - My name is Denise and I was born with arthrogryposis. Desertroses Page - I was born with a condition called arthrogryposis multiplex congenita. Disabilities Unlimited - Bill Micklitz, award winning writer and speaker, was born with a muscle and joint disorder. Emily's Arthrogryposis - Hello my name is Emily and I was born w/ arthrogryposis. Farrah's Rockin Page Farrah's Temple - A little bit about me and who I am. Greg Burns Fine Art Gallery - Greg Burns is an Oklahoma artist whose work in ink and watercolor ranges from historical buildings and homes to Victorian interiors and even landscapes. Jamie-Lee's Arthrogryposis Multiplex Congenita - Includes information, photographs and useful links.

82. Login Arthrogryposis multiplex congenita. amyoplasia. screening abnormality in afetus associated with arthrogryposis multiplex congenita and amyoplasia. http://www.dimed.com/specialista/secure/database/en/docsmanager/dbidparam/2512.a

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83. Login Translate this page Non-lethal arthrogryposis multiplex congenita presenting with cystic in afetus associated with arthrogryposis multiplex congenita and amyoplasia. http://www.dimed.com/specialista/secure/database/docsmanager/dbidparam/1207.aspx

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84. Phase I Scholars The full name of my disability is amyoplasia Arthrogryposis Multiplex congenita.My favorite classes currently are math, science, marching band, jazz band, http://www.washington.edu/doit/Snapshots/2004/phase1.html

Search Directories Reference Tools UW Home ... DO-IT DO-IT resources DO-IT programs DO-IT search DO-IT home page Phase I Scholars Twenty-two Phase I Scholars attended their first DO-IT Summer Study session at the University of Washington in August of 2004. They learned about college life and prepared for college and careers. Throughout the year, they communicate with each other as well as DO-IT participants and DO-IT Mentors. They use the Internet to support their academic studies, and they complete projects in exciting fields that include science, engineering, mathematics, technology, and business. Andrew Laura Lukas Kathleen ... Jessica Andrew '04 Scholar Hey guys. My name is Andrew and I'm going to be a senior at Skyline High School. I'm energetic and easy to talk to. During the school year I'm busy with Choir and performances that I do with my voice teacher. All year I am in training for the track season where I throw the javelin. This year I was seventh in King County for javelin and alternate to State Solo and Ensemble Competition. This summer I attended the Ironwood Throwers Camp. I have Attention Deficit Hyperactivity Disorder (ADHD) and a learning disability in reading and writing. Accommodations, like extra time on tests, have been very helpful. My favorite subjects are math, science, and choir. I hope to major in vocal music or engineering and throw Javelin in college. Laura '04 Scholar My name is Laura. I am 17 and will be a senior at Mercer Island High School this fall. My favorite sports are swimming and tennis. I am active in several youth groups. I enjoy volunteering for a variety of groups and hanging out with my friends; I am a very social person. I was injured in a car accident when I was in 7th grade and as a result of that, I am legally blind in one eye and I suffered a traumatic brain injury. Though I have learned to deal with a lot of the issues surrounding my injuries, I still face challenges both in and out of school. I am looking forward to being a part of the DO-IT program so that I can learn about technology that will assist me with my disabilities and meet new people. My long term goal is to become a teacher.

85. MUMS List Of Disorders - A Arthrogryposis Multiplex congenita (19) *; Arthrogryposis Multiplex congenita,amyoplasia Type (1); Arthrogryposis, Classic (1) *; Arthrogryposis, http://www.netnet.net/mums/mum_a.htm

Return to MUMS Home Page MUMS: List of Disorders A Number in parentheses indicates number of matches. 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) 4A Syndrome(Adrenocortical Insufficiency, Alacrima, Achalasia,Autonomic)(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) *

86. About Ani Samargian Vinson Meet People - ICQ.com Personal Interests. Parenting, I am a mother of a special child. ArthrogryposisMultiplex congenita amyoplasia. Disablities Special Needs http://www.icq.com/whitepages/about_me.php?Uin=39094271

87. Special Child: Disorder Zone Archives - Arthrogryposis Multiplex Congenita Arthrogryposis Multiplex congenita (AMC) is a musculoskeletal disorder characterizedby the presence However, the most common form of AMC is amyoplasia. http://www.specialchild.com/archives/dz-036.html

Disorder Zone Archives Arthrogryposis Multiplex Congenita Dylan Brown Jess Daniel Introduction Arthrogryposis Multiplex Congenita (AMC) is a musculoskeletal disorder characterized by the presence of multiple joint contractures (limitation of the range of motion of a joint) at birth. In some cases, only a few joints may be affected, however, in the classic cases of AMC, hands, wrists, elbows, shoulders, hips, feet, and knees are affected. In the more severe cases, joints in the back and jaw can be affected as well. In addition to having joint contractures, children also experience muscle weakness, which further limits movement. There may be as many as 10 to 20 different arthrogrypotic disorders, all with similar joint manifestations. However, the most common form of AMC is amyoplasia. There are many different causes of AMC, but typically it is a result of either problems with joint growth and development, decreased fetal movement (not enough room in the uterus to move), or problems with spinal development in the first 3 months of pregnancy. AMC occurs in 1 out of every 3,000 live births. In most cases, AMC is not inherited and does not occur more than once in a family. However, in about 30% of the cases, a genetic cause has been identified.

88. Judith G. Hall (www.whonamedit.com) Part I. amyoplasia a common, sporadic condition with congenital contractures.American Journal of Medical Genetics, New York, August 1983, 15(4) 57190. http://www.whonamedit.com/doctor.cfm/533.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Judith G. Hall American human geneticist, born July 3, 1939, Boston. Associated eponyms: Hall type of pseudoachondroplasia A disturbance characterised by severe dwarfism, limb shortening and variable spinal alignment. Hall-Pallister syndrome Distinct malformation with hamartoma in the hypothalamus tract, hypopituitarism, imperforate anus and postaxial polydactyly. Biography: On her Internet site, Judith G. Hall presents herself: I am a clinical geneticist primarily interested in congenital anomalies, genetics of short stature, and connective tissue abnormalities, with a particular interest in the natural history and clinical heterogeneity of these disorders. I have worked extensively on arthrogryposis, various types of dwarfism, Turner syndrome, neural tube defects, and syndrome identification. Since nontraditional patterns of inheritance are seen in many congenital anomalies, I am also involved in defining mosacism, genomic imprinting, parent of origin affects, and mechanisms of disease. My work has involved collaborations with lay groups for specific disease entities and involves explaining and counselling about the consequences of the available care options. It also has involved the development of guidelines for the care of common disorders, such as achondroplasia and Turner syndrome.

89. TheFetus.net - Amyoplasia -Maria Verônica Muñoz Rojas, MD, Luís Flávio Gonç amyoplasia a common, sporadic condition with congenital contractures. Am J MedGenet 1983;15571590. 2. 2.Sells JM, Jaffe KM, Hall JG. http://www.thefetus.net/page.php?id=331

90. THE MERCK MANUAL, Sec. 19, Ch. 261, Congenital Anomalies Vertebral defects include congenital scoliosis, which is rare, Muscle biopsyshows amyoplasia, with fatty and fibrous replacement of tissues. http://www.merck.com/mrkshared/mmanual/section19/chapter261/261g.jsp

91. Arthrogryposis AMC is a nonprogressive congenital neuromuscular syndrome characterized by amyoplasia, characterized by fatty and fibrous tissue replacement of the limb http://www.dpo.uab.edu/~birmie/amc.htm

ARTHROGRYPOSIS MULTIPLEX CONGENITA (AMC) Definition Epidemiology Pathophysiology Etiology ... Reference Page Definition AMC is a nonprogressive congenital neuromuscular syndrome characterized by severe joint contractures, muscle weakness, and fibrosis. Epidemiology AMC occurs in 1 out of every 3000 live births. Amyoplasia, characterized by fatty and fibrous tissue replacement of the limb muscles, is the most common form (43%). Pathophysiology The principle cause of AMC is believed to be decreased fetal movements (akinesia) caused by maternal or fetal abnormalities. It is associated with neurogenic and myopathic disorders. It is believed that the neuropathic form of AMC involves a deterioration in the anterior horn cell leading to muscle weakness and fibrosis. Etiology Several factors are implicated in AMC including hyperthermia of the fetus, prenatal virus, fetal vascular compromise, septum of the uterus, decreased amniotic fluid, muscle and/or connective tissue developmental abnormalities. Clinical Manifestations The primary joints involved (in order of decreasing prevalence) include the foot, hip, wrist, knee, elbow, and shoulder. AMC is typically symmetrical and

92. AMC-tauti - Kehitysvammahuollon Tietopankki ARTHROGRYPOSIS MULTIPLEX congenita AMC, Pienten vammaisryhmienresurssikeskusverkosto A National Support Group for Arthrogryposis Multiplexcongenita http://www.saunalahti.fi/kup/syndroma/amc.htm

Kehitysvammahuollon tietopankki Nivelten jäykistymät, koukkusormet ja -polvet, lonkkavika, sisään kiertyneet olkapäät ja vääntyneet jalkaterät AMC-tauti Arthrogryposis Multiplex Congenita Guérin-Sternin syndrooma Otton syndrooma Rossin syndrooma Nimitys AMC tulee englanninkielisistä sanoista Arthrogryposis Multiplex Congenita. Se tarkoittaa synnynnäistä monioireista nivelten jäykistymäsairautta (amyoplasia). Taudin klassisessa muodossa esiintyy nivelten jäykistymiä ja epämuodostumia; mm. koukkusormet ja -polvet, kieroutuneet lonkat, sisään kiertyneet olkapäät sekä virheasennossa olevat jalkaterät. Myös kitalakihalkiot, sydänviat ja muut epämuodostumat ovat yleisiä. Toisinaan aivot voivat olla epämuodostuneet ja seurauksena on psyykkinen kehitysvammaisuus AMC-lapsia arvioidaan syntyvän suhteessa 1/3.000 kaikista lapsista. Vammautumisista n. 30 % arvioidaan geneettiseksi. Oireiston aiheuttavia geenimutaatioita tunnetaan useita, mm. 9. kromosomin lyhyen varressa (9p13.2-p13.1) ja 5. kromosomin pitkässä varressa (5q35) sekä X-kromosomissa. Nämä ovat liittyneet lihas-, hermo- ja sidekudostauteihin. Oireiston vaikeusaste vaihtelee ja se jakautuu useampaan alatyyppiin.

93. Globe Of Blogs ::: Browse By Weblog Topic ::: Meta ::: Personal Weblog Wife and mother of 4 kids, one with disabilities, Arthrogryposis multiplexcongenita amyoplasia. Location Richmond, Virginia Flag of Virginia http://globeofblogs.com/?x=topic&topic=517&page=150

94. Contractures Worst with CNS involvement 50% death in infancy; Best amyoplasia Finger flexioncontractures Congenital or childhood onset; Elbow wrist http://www.neuro.wustl.edu/neuromuscular/msys/contract.html

Front Search Index Links ... Patient Info CONTRACTURES Contractures with neuromuscular disorders Arthrogryposis Bethlem Myopathy Congenital muscular dystrophy ... Scleroatonic muscular dystrophy (Ullrich) Spinal Muscular Atrophy 5q-linked Congenital X-linked Infantile Tel Hashomer camptodactyly Williams-Beuren syndrome Contractures with myopathy or other neuromuscular disease Congenital Muscular Dystrophy Fukuyama Merosin Deficient Occidental; Normal Merosin With Rigid spine Scleroatonic muscular dystrophy (Ullrich) Dystrophies Dystrophinopathies LGMD 1G LGMD 2A Bethlem Myopathy (Dominant) Emery-Dreifuss Other myopathies Rigid Spine Syndromes Congenital muscular dystrophy LGMD 2A Emery-Dreifuss variant Reducing body Hereditary IBM + Ophthalmoplegia Congenital myopathy with spindle excess King-Denborough ... Myasthenia Gravis: Neonatal Spinal Muscular Atrophy 5q-linked Congenital X-linked Infantile Other Schwartz-Jampel Tel Hashomer camptodactyly Camera-Marugo-Cohen syndrome Dermatomyositis ... Muscle fibrosis due to injections Meperidine Pentazocine Heroin Antibiotics in infants Williams-Beuren syndrome Rhabdomyolysis : Severe Emery-Dreifuss Muscular Dystrophy : Emerin; Chromosome Xq28; Recessive

95. Clinical Orthopaedics And Related Research - UserLogin No patient with amyoplasia (Group I) had congenital vertical talus. The congenitalvertical talus seen in distal arthrogryposis (Group II) was milder than http://www.corronline.com/pt/re/corr/fulltext.00003086-200505000-00005.htm

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96. Willy Nachtmann: Kinder Und Jugendliche Mit Arthrogryposis Multiplex Congenita ( Translate this page Arthrogryposis multiplex connata, kongenitale Arthromyodysplasie, Amyoplasiacongenita, Neuromyopathia congenita oder Fetale Hypokinesie-Sequenz. http://www.school-scout.de/vjk_Arthrogryposis_multiplex_congenita.cfm

Home Lehrer Abitur Abos ... Beenden Kundennummer: Neu hier? Fach: !beliebig! Deutsch Geschichte Mathe Englisch Chemie Erdkunde SoWi Begriff: Geschichte Deutsch Erdkunde SoWi ... Beenden fgdfg MATERIAL Fach: !beliebig! Allgemein Biologie Chemie Deutsch Englisch Erdkunde Französisch Geschichte HSK Jura Kunst Latein Mathe Musik Physik Religion SoWi Begriff: AKTUELLES Materialien im Paket zum einen Bruchteil der Kosten HIER! Unser Gesamtkatalog School-Scout CD's Das Beste für LEHRER ... Interpretationen Die Materialien des Julius Klinkhardt Verlages jetzt online downloaden! Willy Nachtmann: Kinder und Jugendliche mit Arthrogryposis multiplex congenita (AMC) Inhalt: 1. Zum Begriff Arthrogrypose 2. Medizinische Aspekte 2.1 Definition 2.2 Ätiopathogenese 2.3 Klassifikation 2.4 Inzidenz / Prognose 2.5 Symptomatik / Erscheinungsformen 2.6 Diagnostische Möglichkeiten 3. Medizinische und medizinisch-therapeutische Behandlungsmöglichkeiten 3.1 Konservative Therapie 3.2 Operative Therapie 3.3 Spezifische Krankengymnastik / Physiotherapie 3.4 Ergotherapie

97. 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

98. Pages 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 The summary for this Arabic page contains characters that cannot be correctly displayed in this language/character set. http://www.emro.who.int/umd/browsingDic.asp?PageNo=9&char=A

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