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
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
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
Extractions: Search Directories Reference Tools UW Home ... DO-IT DO-IT resources DO-IT programs DO-IT search DO-IT home page 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.
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
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) 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) *
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
Extractions: 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.
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
Extractions: 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. 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.
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
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
Extractions: 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.
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
Extractions: 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.
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
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
Extractions: 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
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
