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         Amyoplasia Congenita:     more detail

21. Roche Lexikon Medizin (4. Aufl.) - Amyoplasia Congenita
Translate this page Amyo pla sia congenita. engl. amyoplasia congenita. Krankheitsbild der Gruppe Arthrogryposis multiplex congenita mit verminderter
http://www.gesundheit.de/roche/ro00000/r1362.html
Amyo pla sia congenita engl.: amyoplasia congenita
Krankheitsbild der Gruppe Arthrogryposis multiplex congenita
Verwandte Themen Arthrogryposis multiplex congenita

22. Arthrogryposis Multiplex Congenita
GuerinStern Syndrome; amyoplasia congenita. General Discussion Arthrogryposis Multiplex Congenita, a rare disorder that is present
http://my.webmd.com/hw/health_guide_atoz/nord211.asp
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You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Arthrogryposis Multiplex Congenita Important It is possible that the main title of the report Arthrogryposis Multiplex Congenita is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • AMC Congenital Multiple Arthrogryposis Fibrous Ankylosis of Multiple Joints
Disorder Subdivisions
  • Neurogenic Arthrogryposis Multiplex Congenita Myopathic Arthrogryposis Multiplex Congenita Guerin-Stern Syndrome Amyoplasia Congenita
General Discussion Resources Human Growth Foundation 997 Glen Cove Avenue Glen Head, NY 11545

23. Arthrogryposis Multiplex Congenita, AMC, Congenital Multiple Arthrogryposis, Fib
Joints, Neurogenic Arthrogryposis Multiplex Congenita, Myopathic Arthrogryposis Multiplex Congenita, GuerinStern Syndrome, amyoplasia congenita,Otto syndrome
http://www.icomm.ca/geneinfo/amc1.htm
Arthrogryposis Multiplex Congenita, AMC, Congenital Multiple Arthrogryposis, Fibrous Ankylosis of Multiple Joints, Neurogenic Arthrogryposis Multiplex Congenita, Myopathic Arthrogryposis Multiplex Congenita, Guerin-Stern Syndrome, Amyoplasia Congenita,Otto syndrome,Rocher-Sheldon syndrome,Rossi syndrome,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
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
HOME
DISORDERS GLOSSARY Arthrogryposis Multiplex Congenita, (AMC)
also known as:
AMC
Congenital Multiple Arthrogryposis
Fibrous Ankylosis of Multiple Joints
Otto syndrome
Rocher-Sheldon syndrome Rossi syndrome 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 Disorder Subdivisions Neurogenic Arthrogryposis Multiplex Congenita Myopathic Arthrogryposis Multiplex Congenita

24. Definitions Of Genetic Disorders-A.
andersen.htm Amyloidosis amylo.htm Amyloidosis of Familial Mediterranean Fever amylo.htm Amylopectinosis andersen.htm amyoplasia congenita amc1.htm Amyotrophic
http://www.icomm.ca/geneinfo/def-a.htm
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
HOME
DISORDERS GLOSSARY
Definitions of Genetic Disorders beginning with the letter A Click on the link next to the disorder to view its definition. A-Beta-Lipoproteinemia abl.htm
A-V avcd.htm
A-V congheart.html
A Beta-2-Microglobulin Amyloidosis amylo.htm
A-T ataxia.htm
alpha.htm

A1AT Deficiency alpha.htm Aagenaes aagen.htm Aarskog syndrome aarsk.htm Aarskog-Scott Syndrome aarsk.htm Aase-smith syndrome aas.htm Aase Syndrome aas.htm AAT alpha.htm AAT Deficiency alpha.htm Abderhalden-Kaufmann-Lignac Syndrome cystinosis.htm Abdominal Muscle Deficiency Syndrome pbs1.htm Abdominal Wall Defect aparosch.htm Abdominal Epilepsy epilepsy.htm Abdominal Migraine cvs1.htm Abductor Spasmodic Dysphonia csd.htm Abductor Spastic Dysphonia csd.htm

25. Dictionary Definition Of AMYOPLASIA CONGENITA
Displaying dictionary terms starting with letter AM amylopsin amylopullulanase amylorrhoea amylose amylosuria amylum amyluria amyocardia amyoesthesia amyoplasia amyoplasia congenita amyostasia amyostatic
http://www.dictionarybarn.com/AMYOPLASIA-CONGENITA.php
Dictionary definition of AMYOPLASIA CONGENITA
Browse Dictionary by alphabet A B C D ... Z Top Words Am antigens
AMA

amacratic

amacrine
...
ambucetamide

Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked.
Synonym: amyoplasia congenita.
Please select first two letters of word you are looking for AA AB AC AD ... AZ fiSearchFormMaxSetId='AX006027'; Top Words ambulacral
ambulacriform

ambulacrum

ambulances
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26. Arthrogryposis Multiplex Congenita
Neurogenic Arthrogryposis Multiplex Congenita; Myopathic Arthrogryposis Multiplex Congenita; GuerinStern Syndrome; amyoplasia congenita. General Discussion.
http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord211

27. Arthrogryposis Multiplex Congenita
RocherSheldon syndrome … Rossi syndrome … amyoplasia congenita … Congenital arthromyodysplastic syndrome … Congenital articular rigidity
http://ibis-birthdefects.org/start/arth.htm
Arthrogryposis Multiplex Congenita
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... Etchings Notice! The theme of this page is beyond the scope of the mission of I.B.I.S. The links shown below are highly selected and of limited scope. AMC Artrogriposis Arthrogryposis Arthrogryposis Multiplex Congenita Congenital Articular Rigidity Congenital Contractures Multiple Congenital Contractures
Special Resources Arthrogryposis Multiplex Congenita
A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Groups [Dutch] [Flemish] [German] [Spanish] [Ukrainian] [*][P] Arthrogryposis Multiplex Congenita Arthrogryposis Arthrogryposis What is it? ... From the Greek literally means "curved or hooked joints." … Used to describe multiple joint contractures present at birth. There are many causes for congenital multiple joint contractures, … The commonest form of arthrogryposis, present in 40% of cases, is a condition called amyoplasia … Lack of movement of intrauterine movement is also responsible, as in oligohydramnios … What are the symptoms? … In the commonest form of arthrogryposis, called amyoplasia, the typical deformities are … Shoulder - internal rotation deformity … Elbow - extension and pronation deformity … Wrist - volar and ulnar deformity … Hand - fingers in fixed flexion, and thumb-in-palm deformity … Hip - flexed, abducted and externally rotated, often dislocated … Knee - flexion deformity … Foot - clubfoot deformity …

28. Dorlands Medical Dictionary
2. myotonic dystrophy. myodystrophia feta¢lis, amyoplasia congenita. myodystrophy (myo·dys·tro·phy) (mi²odis¢trschwa-fe) 1. muscular dystrophy.
http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

29. ARTHROGRYPOSIS : Contact A Family - For Families With Disabled Children: Informa
Arthrogryposis amyoplasia congenita; Arthrogryposis Multiplex Congenita; Otto syndrome. Arthrogryposis Multiplex Congenita (AMC) is
http://www.cafamily.org.uk/Direct/a72.html
printer friendly ARTHROGRYPOSIS home more about us in your area conditions information ... how you can help search this site Did you find this page
helpful?
yes no Arthrogryposis: Amyoplasia Congenita; Arthrogryposis Multiplex Congenita; Otto syndrome Arthrogryposis Multiplex Congenita (AMC) is a term used to describe a baby born with multiple joint contractures and covers a wide range of conditions. The contractures limit the range of movement of the joints. The joints themselves may be fixed in a flexed or extended position. The number of joints affected can range from two or three to almost total involvement, including spine and jaw, resulting in a wide range of disability. AMC is a non-progressive condition with a normal life-span. However, joint contractures are sometimes linked to rare syndromes with limited life expectancy. Although AMC is associated with fetal immobility, the exact causes are not known. Early and specific diagnosis for each case is essential so that appropriate therapy can begin as soon as possible. Such treatment includes physiotherapy (including passive stretching) splinting and surgery. Inheritance patterns
These are variable. In Amyoplasia, the most common form of AMC, there is no significant inheritance risk. Distal arthrogryposis, which primarily affects the hands and feet, is autosomal dominant. However, as there are over one hundred types of AMC, precise diagnosis of individual cases is necessary to establish the risk of possible recurrence.

30. Index A: Contact A Family - For Families With Disabled Children: Information On
Alzheimer s disease Amblyopia see Vision Disorders in Childhood Amyloidosis see Metabolic diseases amyoplasia congenita see Arthrogryposis Amyotrophic Lateral
http://www.cafamily.org.uk/Idx/a.html
printer friendly home more about us in your area ... how you can help search this site Please use the Index below to access the condition on which you require information. If you do not find what you want in the Index then try our search facility in the navigator on the left. 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 Porphyria ALD see Adrenoleukodystrophy ALL see Leukaemia and other allied blood disorders AMC see Arthrogryposis AML see Leukaemia and other allied blood disorders APRT see APS see Hughes syndrome ASA see ASD see Heart Defects ATR-X see Alpha Thalassaemia - Mental Retardation on the X Chromosome Abdominal Exstrophies Abdominal Migraine Abetalipoproteinaemia see Metabolic diseases Achondroplasia Acne Acne Vulgaris see

31. Medical Information Site With Residency Directory, Auctions, Lab
Acidopathies, Congenital 113) Amnesia 114) Amniotic Band Syndrome 115) Amniotic Bands 116) Amoebiasis 117) Amyloidosis 118) amyoplasia congenita 119) Amyotonia
http://www.residency.info/dxenc/index.php?v=2&l=A

32. Neurologic Development In Children
This is the case report of a 6 year old boy who suffers from arthrogryposis multiplex congenita (AMC), also known as amyoplasia congenita is a congenital lack
http://www.chiroclinic.com.au/conditions/child_dev.shtml
Neurologic Development in Children Birth trauma, antibiotic abuse, vaccine reaction: a single case report. Phillips, CJ ICA Review Sept/Oct 1996 Fourteen month old female with delayed development, hypotonia, dysarthria, excessive cranial molding, photophobia, loss of visual motor control, history of excessive antibiotic therapy and adverse reaction to vaccinations. After one week of chiropractic and cranio-sacral therapy: Decreased symptoms of photophobia, increased muscle tone and ability to sit on mother's lap with minimal support, no pain when held erect and increased muscle strength allowing her to be held against her parent's shoulder with normal head control (previously flopped backwards if not supported), increased visual acuity, decrease in athetoid movements of arms, hands and fingers, immediate change in mood with a calmer, happier disposition.
Effect of osteopathic medical management on neurologic development in children. Frymann VM, Carney RD, Springall P. JAOA, 92;729-744, 1992. Neurologic performance (sensory performance, manual competence, mobility, and spoken language) significantly improved after treatment in children with defined neurologic problems...improvement continued to occur over several months....children with neurologic
problems have exhibited significantly improved sensory and motor functions."

33. Syndrome DB - Table Of Contents
embryopathy aminopterinlike syndrome aminopterin-like syndrome without aminopterin Amish brittle hair syndrome Amsterdam type amyoplasia congenita anal-ear
http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_a.html
Multiple Congenital Anomaly/Mental Retardation Syndromes
Table of Contents
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A
B C ... Z
A
Aarskog syndrome
Aarskog-Scott syndrome (ASS)

abdominal muscle deficiency anomalad

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

35. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/A
Amputee@ (36); Amyloidosis@ (16); amyoplasia congenita@ (99); Amyotrophic Lateral Sclerosis@ (64); Anal Cancer@ (10); Anal Fissures@ (2
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/A
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36. Pediatrics: Treatment Of Pain With Gabapentin In A Neonate
shown to be effective in the treatment of neuropathic pain in adults2 and children.3 We report the case of a neonate with amyoplasia congenita resulting in
http://articles.findarticles.com/p/articles/mi_m0950/is_2_108/ai_77480792
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Pediatrics
August, 2001 by Martin O. Behm Gregory L. Kearns
ABBREVIATIONS. GBP, gabapentin; GABA, gamma-aminobutyric acid; DOL, day of life. 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.[1] Recently, GBP has been shown to be effective in the treatment of neuropathic pain in adults[2] and children.[3] We report the case of a neonate with amyoplasia congenita resulting in severe contractures and dislocated joints who was successfully and safely treated with GBP to relieve pain. CASE REPORT Symptomatic assessment on DOL 4 illustrated apparent failure of acetaminophen, which prompted its discontinuation and the initiation of ibuprofen therapy (ibuprofen oral suspension) at a dose of 10 mg/kg every 6 hours. At this same time, an electromyeolgram was performed. It revealed that the neurologic problems were axonal in nature and represented a static process. The Genetics Department was consulted and initial results indicated a pericentric inversion of chromosome 8. Additionally, consultation from the Orthopaedic Surgery Service was obtained, which recommended mobilization of muscle tissue as opposed to surgical intervention or the use of braces/splints. During this time, the diagnosis was refined to amyoplasia congenita, a sporadic abnormality most likely caused by hypotension in the developing fetal spinal cord at a time when anterior horn cells are susceptible to insults.[4]

37. Sjukdom, Sjukdomslista På Engelska, Michel Tandläkare Ta Hand Om Dig
Altophobia. Alzheimer s. Amblyopia. Amputee. Amyloidosis. amyoplasia congenita. Amyotrophic Lateral Sclerosis. Anal Fissures. Anemia. Anencephaly. Aneurysm.
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38. Genetic And Rare Diseases Information Center - Office Of Rare Diseases
Synonyms Arthrogryposis multiplex congenita (AMC). Otto syndrome. RocherSheldon syndrome. Rossi syndrome. amyoplasia congenita. Disease Information.
http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=8412

39. Centre For Arab Genomic Studies
Amish brittle hair syndrome, Amsterdam type, amyoplasia congenita, analear-renal-radial malformation syndrome, Andermann syndrome, Anderson disease,
http://www.cags.org.ae/cags_html/HTML/EN/diseases.php

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DISEASES A B C D ... Z Disease Omim Aarskog syndrome Aarskog-Scott syndrome (ASS) abdominal muscle deficiency anomalad abdominal muscle deficiency syndrome ... Z

40. Yes Medical Information On Ailments, Personal And Family Health Matters - Yes Me
1); Alzheimer s (136); Amblyopia (7); Amebiasis (19); Amputee (40). Amyloidosis (16); amyoplasia congenita (98); Amyotrophic Lateral Sclerosis
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