Extractions: For Researchers For Librarians Authors: Shenoy M. ; Marlow N.; Stewart R. Source: Acta Paediatrica , Volume 88, Number 12, 7 December 1999, pp. 1405-1406(2) Publisher: Taylor and Francis Ltd View Table of Contents full text options Free trial available! Abstract: A newborn girl with amyoplasia congenita and non-duodenal intestinal atresia is reported. Amyoplasia is a rare sporadic condition seen more commonly in identical twins, who are discordantly affected. It is characterised by absence of limb muscles that are replaced by fibrous and fatty tissue. Non-duodenal intestinal atresias have been shown to be caused by vascular interruption. The occurrence of both these conditions together suggests a common etiology. Language: English Document Type: Research article Affiliations: The full text article is available for purchase $38.12 plus tax
ARTHROGRYPOSIS Contact A Family - For Families With Disabled yes no Arthrogryposis Arthrogryposis Multiplex Congenita; AMC The commonest cause of AMC is amyoplasia (lack of muscle formation). http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
IngentaConnect Table Of Contents: Acta Paediatrica amyoplasia congenita and intestinal atresia a common etiology pp. 14051406(2)Authors Shenoy M.; Marlow N.; Stewart R. Different responses to granulocyte http://www.ingentaconnect.com/content/tandf/spae/1999/00000088/00000012
Arthrogryposis Multiplex Congenita Patients with amyoplasia congenita do not have evidence of brain, cardiac, amyoplasia congenita is the final diagnosis in about onethird of neonates http://pediatricneuro.com/alfonso/pg163.htm
Extractions: Patients with amyoplasia congenita do not have evidence of brain, cardiac, or genitourinary tract abnormality. Bowel atresia and gastroschisis have been reported. The cause of amyoplasia congenita is unknown. Fetal spinal cord disruption due to systemic hypotension producing anterior horn cell ischemia is the most likely explanation. Amyoplasia congenita is a sporadic condition. This is an important condition to recognize since the chances of recurrence are low and the prognosis is good. Muscle biopsies may show evidence of myopathy and neuropathy. Amyoplasia congenita is the final diagnosis in about one-third of neonates with arthrogryposis. Spinal Cord Abnormalities Traumatic spinal cord injury usually occurs during delivery. It should be suspected if no cause for arthrogryposis is found and there are no signs of brain or brainstem involvement. Magnetic resonance imaging of the spine is indicated. Arthrogryposis of the lower extremities has been reported with lumbosacral meningocele (Figure 163.1) and with sacral agenesis. A B Figure 163.1.
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Arthrogryposis Multiplex Congenita Figure 162.1 amyoplasia congenita. A Typical facial appearance. B Abnormalposition of the limbs. MainMenu Back Next Index. http://pediatricneuro.com/alfonso/pg162.htm
Extractions: Marden-Walker syndrome or cerebro-oculo-facio-skeletal syndrome is characterized by the presence of a fixed facial expression, blepharophinosis, micrognathia, and multiple joint contractures from birth. Brain and posterior fossa malformations are frequent. Dandy-Walker abnormality and brainstem hypotonia may occur. It is an autosomal recessive condition. SPINAL CORD Amyoplasia Congenita
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Netter Medical Images - Search Results For Amyoplasia Congenita Netterimages.com The most trusted name in medical illustration PRICING ARTISTSREGISTER LOGIN. SEARCH RESULTS. 1 IMAGES IN SELECTION PAGE 1 OF 1 http://www.netterimages.com/image/list.htm?s=amyoplasia congenita
Extractions: 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
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Entrez PubMed management of significant knee deformity in 44 knees of 22 patients sufferingfrom classical arthrogryposis multiplex congenita (amyoplasia congenita). http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9
Entrez PubMed Comments on amyoplasia congenitaLike Condition and Maternal Malathion Exposure Is all Amyoplasia Amyoplasia? Hall JG. Publication Types http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3
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. Amyoplasia congenita, arthrogryposis multiplex congenita, arthrogryposis syndrome, arthromyodysplasia congenita, congenital arthromyoplastic syndrome, congenital articular rigidity, congenital contractures of extremities, multiple congenital articular rigidity, multiple congenital contractures, myodysplasia fibrosa multiplex, myodysplasia fetalis deformans, myodystrophia fetalis deformans, neuro-arthromyodysplasia, pterygium universalis, pterygo-arthromyodysplasia congenita.
Arthrogryposis Multiplex Congenita Arthrogryposis Multiplex Congenita, a rare disorder that is present at birth Multiplex Congenita; GuerinStern Syndrome; amyoplasia congenita http://www.bchealthguide.org/kbase/nord/nord211.htm
Sign/View Abby S Guestbook - ForAbby.Com - Arthrogryposis My baby girl, Emily, has amyoplasia congenita. She is 41/2 months old and hashad casts I have a 14-month-old granddaughter with amyoplasia congenita. http://www.forabby.com/guestbook.htm