81. MUMS List Of Disorders - A Multiplex congenita (19) *; Arthrogryposis Multiplex congenita, amyoplasia Type (1); Arthrogryposis, Classic (1) *; Arthrogryposis, Distal 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) *

82. Blackwell Synergy - Cookie Absent 9, Hall JG, Reed SD, Driscoll EP Part I. amyoplasia. A common, sporadic condition with congenital contractures. Am. J. Med. Genet. http://www.blackwell-synergy.com/links/doi/10.1046/j.1440-1754.1998.00296.x/full

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

83. Blackwell Synergy - Cookie Absent Arthrogryposis multiplex congenita may be classified by the pattern of involvement of the joints, amyoplasia being the most common form comprising onethird of http://www.blackwell-synergy.com/links/doi/10.1046/j.1471-0528.2002.01170.x/full

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

84. Arthrogryposis Multiplex Congenita (AMC) - Homepages Of People Who Have A Disabi of a woman with multiple disabilities, including arthrogryposis multiplex congenita. of 2002 with a rare condition called arthrogryposis (amyoplasia) at first http://www.wtmy.com/manasota/disabled-homepages/arthrogryposi.html

Personal Pages of People who have Arthrogryposis Multiplex Congenita (AMC) Arthrogryposis: A Text Atlas Amazon.com has Books about Arthrogryposis Amazon.com has books about Arthrogryposis Home What's New Sponsors/ ... Alicia Hoppus - Girl from Nebraska with arthrogryposis. Alina Echemendia - My world. Andrea Rust Andrea's World - My life story with arthrogryposis. AMC Roy - Roy Silvernail"s Page - my name is peter van hemert,i live in the hague,holland and i was born with arthrogryposis. Art By Lori - I am a disabled artist who paints by holding a brush in my mouth. Art Carlson - I'm a handicapped comedian based out of Denver, Colorado. 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. Clay's arthrogryposis homepage Colby's Arthrogryposis Multiplex Congenita Information Page - Personal site with information on AMC. confoozled.com

85. NEUROMUSCULAR DISORDERS Arthrogryposis Multiplex congenita, amyoplasia This is a non progressive disorder with multiple, congenitally rigid joints. It http://www.worldortho.com/database/etext/neuromuscular.html

NEUROMUSCULAR DISORDERS Information relating to all listed Neuromuscular disorders is given, in the ensuring text. HEREDITARY NEUROPATHIES The Hereditary Neuropathies category includes all disorders associated with multiple G.N.S. lesions This involves motor and sensory defects. It is a spinocerebellar degenerative disease with manifests before age 10. The symptoms include nystagmus, casus foot, cardiomyopathy, scoliosis and a distinct change in gait. Charcot - Marie - Tooth Disease [Peroneal Muscular Atrophy] There are two forms, one manifesting during teenage years [a hypertrophic form] and a neuronal form manifesting in later life. Patients suffering the hypertrophic form exhibit peroneal weakness, hammer toes causing corns and callouses, pes cavus and stork legs. Treatment includes plantar release triple arthrodesis versus calcaneal, posterior tibial tendon transfer and possibly, metatarsal osteotomies. This form involves motor defects much more than sensory defects Dejerine - Sottas Disease - AR.

86. Judith G. Hall (www.whonamedit.com) JG Hall, SD Reed, EP Driscoll Part I. amyoplasia a common, sporadic condition with congenital contractures. American Journal of 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. 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.

87. TheFetus.net - Amyoplasia -Maria Verônica Muñoz Rojas, MD, Luís Flávio Gonç 2 References 1. Hall JG, Reed SD, Driscoll EP. Part 1. amyoplasia a common, sporadic condition with congenital contractures. Am J Med Genet 1983;15571590. http://www.thefetus.net/page.php?id=331

88. THE MERCK MANUAL, Sec. 19, Ch. 261, Congenital Anomalies Congenital myopathies, anterior horn cell disease, and maternal myasthenia gravis have been proposed as causes of the associated amyoplasia. http://www.merck.com/mrkshared/mmanual/section19/chapter261/261g.jsp

89. Heilpflanzen-Welt - Die Welt Der Heilpflanzen! Translate this page http://01.dokmed.de/3778.htm

90. Birth Disorder Information Directory - M Craniosynostosis) Congenital heart disease ptosis hypodontia craniosynostosis. Meier Rotschild Syndrome (amyoplasia Mandibulofacial Dysostosis) http://www.bdid.com/defectm.htm

HOME M Machado Joseph Disease (Autosomic Dominant Spinocerebellar Ataxia, Autosomic Dominant Cerebellar Ataxia, Cerebelloolivary Atrophy, Olivopontocerebellar Atrophy, Pierre Marie Cerebellar Ataxia) List of Sites Macrencephaly List of Sites Macrocephaly List of Sites Macrodactyly/Megalodactyly Macrodactly of the Right Foot Macrodactyly of Both Hands and Foot Associated with Cutaneous Hemangiomata MEGALODACTYLY Macroglossia Macroglossia (Includes Ultrasounds and Photos) Also see Beckwith Wiedemann Syndrome Blomstrand Syndrome Congenital Hypothyroidism Mucopolysaccharidosis and Simpson Golabi Behmel Syndrome Macrogyria MACROGYRIA Asperger's Syndrome Macular Dystrophy Vitelliform See Best Disease/Macular Dystrophy Atypical MACULAR DYSTROPHY, ATYPICAL VITELLIFORM; VMD1 Macules Hereditary Congenital Hypopigmented and Hyperpigmented See Westerhof Beemer Cormane Syndrome Madelung's Deformity See Leri Weill Syndrome Majewski Syndrome See Short Rib-Polydactyly Syndrome, Type IV Mal de Meleda See Meleda Disease Male Pseudohermaphroditism Due to 5-Alpha-Reductase Deficiency See Pseudovaginal Perineoscrotal Hypospadias Due to Androgen Insensitivity See Androgen Insensitivity Syndrome Male Turner Syndrome See Noonan Syndrome Malignant Hyperthermia See Hyperthermia, Malignant

91. Arthrogryposis Definition AMC is a nonprogressive congenital neuromuscular syndrome characterized by amyoplasia, characterized by fatty and fibrous tissue replacement of the 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. Roche Lexikon Medizin (4. Aufl.) - Arthrogryposis Multiplex Congenita congenital arthrogryposis multiplex; arthromyodysplasia. http://www.gesundheit.de/roche/ro00000/r2287.html

Arthro gry po sis multi plex congenita Arthromyodysplasia congenita, G *-S TERN * Syndrom engl.: congenital arthrogryposis multiplex; arthromyodysplasia path-anat Verwandte Themen Aase*-Smith* Syndrom Amyoplasia congenita Arthromyodysplasie Gliederstarre ... Starre

93. Arthrogryposis Of The Knee: MRI Findings - Eurorad - Clinical Case 2405 - Reside The term arthrogryposis” stands for a very heterogeneous group of disorders encompassing multiple congenital muscular contractures 2, 4. The main cause is http://www.eurorad.org/case.cfm?uid=2405

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