61. MizMoz Directory - Conditions And Diseases Conditions And Diseases Amyloidosis (16) »amyoplasia congenita (98) »Amyotrophic Lateral Sclerosis (64) »Anal Cancer (10) »Anal Fissures (2) »Anemia (95) »Anencephaly (15 http://www.mizmoz.com/dir/Health/Conditions_and_Diseases/A/

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62. UBEP 2000 Seventh Annual Undergraduate Research Symposium In addition to resistance, some treatments have been linked to or claimed to have many side effects for humans including amyoplasia congenita in pregnancy http://lsvl.la.asu.edu/ubep2000/abstracts/abst65/

Shifting Strategies for Dealing with Head Lice Infestation: A Case Study in Guadalupe Farshad F. Marvasti and Jane A. Maienschein Departments of Biology and Philosophy, Arizona State University Abstract: In any given urban area with ample population congestion, there is a problem with head lice infestation. Public policies in place to deal with this medical problem generally involve the use of caustic chemicals and a "No-Nits" policy that keeps affected children out-of-school until their parents have eliminated all lice and their eggs. The biology, ecology, and evolutionary history of head lice, however, call into question these practices and suggest shifting our treatment programs from eradication to management process. Evidence for this shift includes the persistence of head lice and the development of strains resistant to conventional chemical treatments. To discover how this shift works, we aim to evaluate and apply conclusions to the community of Guadalupe as a case-study. Introduction: Recognized for thousands of years as parasites, the remains of head lice have been found throughout the world's history from pre-Columbian Peru to ancient Egypt around 5000 years ago (Hoeppli, 1959; Parish 1985; and Zinsser, 1935). Before the development of microscopy, widespread belief held lice to be spontaneously generated from dirt or decomposing sweat (Burgess, 1995). We now know that the head louse

63. Association Des Amis De S Myasthéniques Du Maroc Forum Web De Discussion S Translate this page dystrophie musculaire. En anglais amyoplasia congenita Terme issu de arthron articulations, et de grupos recourbé. Synonymes http://www.rezoweb.com/forum/sante/myastheniagravi/594.shtml

Recherche dans le forum Envoyer un message Forum myastheniagravi F.A.Q. Archives (3 visiteurs) Modification: 4/4/2004 Création: 27/7/2001 SANTE MALADIE MEDECIN MAROC NEUROLOGIE MYASTHENIE HASSAN_II MOHAMMED_VI IDRISSI MAIDOC2 MAIDOC MESTINON MYTELASE TEGELINE IMMUNOGLOBULINES PLASMAPHERESE THYMUS ASSOCIATION Re: maladie de l arthrogrypose Envoi de DR IDRISSI MY AHMED le 29 Octobre 2002 01:18:46: Réponse à: maladie de l arthrogrypose envoi de eva le 27 Octobre 2002 18:32:11: Arthrogrypose voir également aberration chromosomique, dystrophie musculaire. En anglais : amyoplasia congenita Terme issu de arthron : articulations, et de grupos : recourbé. Synonymes : myodystrophie fœtale déformante, amyoplasie congénitale, raideur articulaire congénitale, myodysplasie ou myodystrophie constitutionnelle (désuètes) Syndrome (ensemble de signes) congénital (existant à la naissance) et apparaissant parfois dès la grossesse, se caractérisant par des raideurs multiples des articulations, plus ou moins symétriques et le plus souvent en flexion (fermeture). On estime sa fréquence à 1 pour 3000 naissances.

64. AMYOPLASIA CONGENITA // Medical-Conditions.org // Medical Conditions Open Directory Health Conditions and Diseases A Alzheimer s@ (134); Amblyopia@ (7); Amebiasis@ (19); Amputee@ (40). Amyloidosis@ (16); amyoplasia congenita@ (98); Amyotrophic Lateral http://www.medical-conditions.org/?q=Amyoplasia Congenita

65. Last Updated 15.03.2001 BRCA1 carriers; Aetiological factors in neonatal cholestasis; amyoplasia congenita Picture of the Month; Bone marrow cytogenetic http://www.rusmedserv.com/genetics/review/rev1503.htm

Last Updated 15.03.2001 A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers Aetiological factors in neonatal cholestasis Amyoplasia Congenita - Picture of the Month Bone marrow cytogenetic abnormalities of aplastic anemia ... Treatment of 193 Episodes of Laryngeal Edema With C1 Inhibitor Concentrate in Patients With Hereditary Angioedema

66. Heilpflanzen-Welt - Die Welt Der Heilpflanzen! Translate this page Amyloidkörper Amyloidose Amyloid-Polyneuropathie, familiäre Amylopektin Amylopektinose absolut Amylose Amylum amyoplasia congenita amyostatisches Syndrom http://00.mediz1n.de/

67. Heilpflanzen-Welt - Die Welt Der Heilpflanzen! amyoplasia congenita (PubMed; engl.). http://unsere.gesundheit.nu/a/a1973.htm

68. PubMed Medline Query of the lethal form of arthrogryposis multiplex congenita. The existence of ultrasonographic abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia. http://www.sonnet.com/avenues/medl9798.html

Medline Abstracts, Arthrogryposis, 1997-98 Clin Genet 1998 Sep;54(3):224-30 Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25>qter deletion. Lukusa T, Devriendt K, Holvoet M, Fryns JP Center for Human Genetics, University Hospital of Leuven, Belgium. We present the first report of chromosomal rearrangement involving chromosomes 4, 10 and 12. The proband was a 42-year-old woman with severe mental retardation and multiple congenital anomalies. The most striking physical anomalies were upper limb contractures resulting in distal arthrogryposis. As upper limb flexion contractures have been previously reported in individuals with partial distal 10q deletion, this sign should be considered as part of the clinical manifestations of 10q25>qter monosomy. PMID: 9788726, UI: 99002775 Fetal Diagn Ther 1998 Jul;13(4):244-249 Congenital Rapidly Fatal Form of Nemaline Myopathy with Fetal Hydrops and Arthrogryposis. a case report and review. Vardon D, Chau C, Sigodi S, Figarella-Branger D, Boubli L

69. Arthrogryposis Multiplex Congenita limbs. In 1923, Stern coined the term arthrogryposis multiplex congenita. In 1983, Hall and colleagues named the most common type of the disease amyoplasia. http://www.ortho.hyperguides.com/Tutorials/pediatric_ort/Arthrogryposis/tutorial

window.location="http://www.ortho.hyperguides.com/"; Arthrogryposis Multiplex Congenita Nigel W. Sparks, MD Background and Diagnosis Clinical Features Treatment Bibliography Background and Diagnosis Arthrogryposis multiplex congenita is a nonprogressive disease that consists of two or more different joint contractures present at birth. There are more than 150 different conditions that are classified under the term arthrogryposis. Causes of arthrogryposis may include abnormalities of muscle, nerve, connective tissue, or limitation of movement in utero. The majority of this tutorial will focus on the most common form of arthrogryposis, amyoplasia. Other disorders in the arthrogrypotic syndromes include Larson’s syndrome, distal arthrogryposis syndrome, and multiple pterygium syndrome. In 1841, Adolf Wilhelm Otto named the disease congenital myodystrophy. He described the patient as a "human wonder with curved limbs." In 1923, Stern coined the term arthrogryposis multiplex congenita. In 1983, Hall and colleagues named the most common type of the disease amyoplasia. Amyoplasia consists of multiple joint contractures, which are symmetrical in positioning of the limbs. The etiology does not have a genetic basis but is sporadic in nature. There have been reports of epidemics in the 1960s in areas of eastern Europe and Great Britain. There seems to be an association with a decrease of anterior horn cells and other neural elements of the spinal cord. There is also a questionable relationship to oligohydramnios.

70. Arthrogryposis Multiplex Congenita Arthrogryposis Multiplex congenita. Nigel W. Sparks, MD. What percentage of patients born with amyoplasia will have fractures of some type at birth http://www.ortho.hyperguides.com/Tutorials/pediatric_ort/Arthrogryposis/pretest.

window.location="http://www.ortho.hyperguides.com/"; Arthrogryposis Multiplex Congenita Nigel W. Sparks, MD What percentage of patients born with amyoplasia will have fractures of some type at birth: (Click on an answer to see if it is correct)

71. Dorlands Medical Dictionary amyoplasia conge¢nita, a generalized lack of muscular development and growth called congenital multiple arthrogryposis and arthrogryposis multiplex congenita. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

72. Wheeless' Textbook Of Orthopaedics Arthrogryposis Multiplex congenita (amyoplasia). Discussion - musculoskeletal dz is characterized by congenital immobility of multiple joints. http://www.wheelessonline.com/o12/110.htm

Main Menu Home Page Arthrogryposis Multiplex Congenita: (Amyoplasia) - Discussion: - Clinical Presentation: - affected patients typically have normal facies, normal intelligence, multiple joint contractures, and no viceral abnormalities; - distal joints are usually affected more severely; - classic arthrogrypotic deformities are present at birth; - note that it is common for newborns to display mild elbow contractures, which should not be confused with arthrogryposis; - Joint motion limitation in newborns. MM Hoffer. CORR. Vol 148. 1980. p 94-96. - diff dx: myelomeningocele ; - moebius syndrome; - larsen's sydndrome (multiple joint dislocations, esp knees); - Pena Shokeir syndrome (growth deficiency, unusual facial features, multiple ankylosis; - camptodactyly (when only a finger is involved); - talipes equinovarus; - congenital myasthenia gravis; - whistling face syndrome; - Initial Workup: - evaluation should include neurologic studies, enzymes tests, and muscle biopsy (at 3-4 months); -

73. Congenital Fiber Type Disproportion No one in either my or my husband s families ever had such a disorder. Molly was diagnosed with Arthrogryposis Multiplex congenita amyoplasia. http://www.mis.dreamhost.com/cftd/

Congenital Fiber Type Disproportion **Important** The information in this page and in the Rare Disease Database is provided for educational purposes only. It should not be used for diagnostic or treatment purposes. If you wish to obtain more detailed information about this disorder, please contact your personal physician and/or the agencies listed in the "Resources" section of this page. Overview What is It? Clinical Features Causes Affected Population ... Other Links What is It? The term congenital fiber type disproportion was first used by a scientist in 1965 to describe a group of hypotonic children with relative type 1 fiber smallness. The fairly uniform clinical presentation, a possible familial incidence, a relatively good prognosis, and a possible common pathophysiological mechanism suggested that it was a disease entity. Presently it is best to regard disproportion in muscle fiber size with 1 fiber smallness, or hypotrophy, as a pathological pattern that can occur in congenital myopathies and also in many other conditions. It is a rare muscle disease that is apparent at birth. Congenital fiber type disproportion is also known as: CFTD Atrophy of Type I Fibers Myopathy of Congenital Fiber Type Disproportion Myopathy, Congenital, With Fiber-Type Disproportion

74. AMC-tauti tulee englanninkielisistä sanoista Arthrogryposis Multiplex congenita. Se tarkoittaa synnynnäistä monioireista nivelten jäykistymäsairautta (amyoplasia). 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 1/3000 kaikista lapsista. Vammautumisista n. 30 % arvioidaan perinnöllisiksi . Oireiston aiheuttavia geenimutaatioita tunnetaan useita, mm. 9. kromosomin lyhyen varressa (9p13.2-p13.1) ja 5. kromosomin pitkässä varressa (5q35) sekä X-kromosomissa. Fysioterapeuttisilla ja kirurgisilla hoidoilla voidaan huomattavasti auttaa AMC-vammaisia. Sairauden vaikeusaste vaihtelee ja se jakautuu useampaan alatyyppiin.

75. Genetic And Rare Diseases Information Center - Office Of Rare Diseases Amylopectinosis. amyoplasia. amyoplasia mandibulofacial dysostosis. Amyotonia congenita. Amyotrophic lateral sclerosis. Anablephobia. Anaplastic thyroid cancer. http://ord.aspensys.com/asp/diseases/diseases.asp?this=A

76. List Of Rare Diseases Starting With A mandibulofacial dysostosis; amyoplasia; Amyotonia congenita; Amyotrophic lateral sclerosis; Anablephobia; Anaphylaxis; Anaplastic thyroid http://www.fact-index.com/l/li/list_of_rare_diseases_starting_with_a.html

Main Page See live article Alphabetical index List of rare diseases starting with A This list of rare diseases was originally taken from the NIH public domain resource at http://ord.aspensys.com/asp/diseases/diseases.asp A B C D E ... Z Table of contents 1 Aa-Ad 2 Ae-Ah 3 Ai-Al 4 Am-Ap ... 6 At-Az Aa-Ad Aagenaes syndrome Aarskog Ose Pande syndrome Aarskog syndrome Aase Smith syndrome Aase syndrome ABCD syndrome Abdallat Davis Farrage syndrome Abdominal aortic aneurysm Abdominal cystic lymphangioma Abdominal defects Abdominal musculature absent microphthalmia joint laxity Abdominal neoplasms Aberrant subclavian artery Ablepharon macrostomia syndrome Ablutophobia Abnormal systemic venous return Abruzzo Erickson syndrome Absence of Gluteal muscle Absence of tibia with polydactyly Absent corpus callosum cataract immunodeficiency Absent T lymphocytes Acalvaria Acanthocheilonemiasis Acanthocytosis chorea Acanthocytosis Acanthosis nigricans muscle cramps acral enlargement Acarophobia Acatalasemia Accessory deep peroneal nerve Accessory Navicular bone Accessory pancreas Achalasia alacrimia syndrome Achalasia microcephaly Achalasia, familial esophageal

77. Acid Maltase Deficiency (209) 9283688. avenues@sonnet.com. http//www.sonnet.com/avenues. amyoplasia, congenita. Asthma Allergy. Allergy and Asthma Network Mothers of Asthmatics. http://www.as.wvu.edu/~scidis/organizationA_B.html

Specific Resources about Types of Disabilities Acid Maltase Deficiency (AMDA)Acid Maltase Deficiency Assoc. PO Box 700248 San Antonio, TX 78270-0248 (210) 490-7161 (fax) tianrama@aol.com http://www.amda-pompe.org Acidemia, Organic Organic Acidemia Association 13210 35th Ave. N. Plymouth, MN 55441 (763) 694-0017 (fax) oaanews@aol.com http://www.oaanews.org Includes: Isovaleric Acidemia Methylmalonic Acidemia Propionic Acidemia Alaninuria Acoustic Neuroma Acoustic Neuroma Association 600 Peachtree Pkwy., Ste. 108 Cumming, GA 30041 (770) 205-0239 (fax) anausa@aol.com http://www.anausa.org Adrenal Disorders National Adrenal Disease Foundation 505 Northern Blvd. Great Neck, NY 11021 NADFMAIL@aol.com http://medhelp.org.www.nadf Includes: 17-20-Desmolase Deficiency 17-Alpha-Hydroxylase Deficiency 17-Hydroxylase Deficiency Acth Deficiency Addison Disease Adrenal Cortex Male Pseudohermaphroditism Adrenocorticotropic Hormone Deficiency Adrenogenital Syndrome Star Protein Deficiency Agenesis of the Corpus Callosum ACC Network 5749 Merill Hall, Rm. 118 University of Maine Orono, ME 04469-5749

78. California Chapter IX a specific disease (Table 1). Unfortunately, the distinction between arthrogryposis multiplex congenita (now commonly referred to as amyoplasia) and other http://aap-ca.com/CA_Pediatrician_Fall_2002x3.htm

Home Home District About Us Leadership Meetings Resolutions Membership To Join Benefits Legislation Priority Issues Bill Tracking Your AAP Legislative Contact News CA Pediatrician The CA Resident Press Releases AAP-CA Updates Resources Web Sites AAP Policy California Pediatrician is pleased to present the following articles and additional material, which have not appeared in printed format. To receive a printed copy of California Pediatrician, contact the District office at (510) 559-8383. Letters to the editor are appreciated and encouraged. To contact the editor, click on the following link: Send to Editor Fall 2002 Articles - Section 3 District Report AAP-CA Successful in Protecting Priority Pediatric Components of State Budget Burton F. Willis, M.D., AAP-CA District Chair Kris Calvin, M.A., AAP-CA Executive Director Arthrogryposis and Amyoplasia Robert M. Bernstein, M.D.

79. Special Child: Disorder Zone Archives - Arthrogryposis Multiplex Congenita Arthrogryposis Multiplex congenita (AMC) is a musculoskeletal disorder characterized by the presence of 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.

80. Arthrogryposis the years, including arthrogryposis multiple congenita, multiple congenital contractures, amyoplasia, myodystrophica congenita, arthromyodysplasia congenita http://www.shrinershq.org/patientedu/arthrogryposis1.html

Home Shrine Shriners Hospitals Hospital Directory ... Next STRAIGHT TALK ABOUT CURVED JOINTS Help for Patients with Arthrogryposis Sixteen-year-old Jennifer Weaver, an arthrogryposis patient at Shriners Hospitals, exercises daily to improve muscle tone and body strength. Don't offer to open a door or carry books or a lunch tray for Jennifer Weaver. She'd rather do it herself, thank you. Although she admires chivalry, Jennifer cherishes her hard-earned independence even more. Born with a rare and crippling condition called arthrogryposis, 16-year-old Jennifer has managed to overcome many of the physical limitations that are now a distant memory. "I knew when she threw her crutches across the room at age 3 while yelling 'I hate those things!' that she was a fighter," recalls Jennifer's mom Pam. Today, Jennifer is manager of her high school drill team, a star soloist in the school choir and works out daily at the gym. About the only physical challenge she encounters these days are stairs, which can be tricky to negotiate with leg braces. Often at school, Jennifer's football playing buddies scoop her up, toss her over their shoulders and run up the stairs, while petite, 100 pound Jennifer yells in protest that she can do it herself. What is arthrogryposis?

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