61. Am : On Medical Dictionary Online amyoplasia congenita Amyotonia Congenita Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis With Dementia Amyotrophic Lateral Sclerosis http://www.online-medical-dictionary.org/am.asp?q=~Am

62. D Lindhout Publications amyoplasia congenitalike condition and maternal malathion exposure. Lindhout D, Hageman G. amyoplasia congenita and maternal malathion exposure. http://humgen.med.uu.nl/addresses/people/curriculum/Lindhout pubs.html

Publications by D. Lindhout, M.D., Ph.D. CONTENTS I Articles in international peer-reviewed scientific journals II Articles in Dutch peer-reviewed journals III Chapters in books (English) IV Chapters in books (Dutch) ... VI Educational articles last updated October 2002 I Articles in international peer-reviewed scientific journals 1. Lindhout D, Barth PG, Valk J, Boen-Tan TN. The Joubert syndrome associated with bilateral chorioretinal coloboma. Eur J Pediatr 1980;134:173-176. 2. Lindhout D. The Joubert syndrome associated with bilateral chorioretinal coloboma (letter). Eur J Pediatr 1981;137:101-102. 3. Lindhout D, Meinardi H. False-negative pregnancy test in women taking carbamazepine (letter) Lancet 1982;ii:505. 4. Heimans JJ, Lindhout D, Huisman UW, Kwee ML, Visser SL, Whitton HW. H-reflex studies in a family with possibly X-linked neuronal Charcot-Marie-Tooth disease. Clin Neurol Neurosurg 1982;84:147-158. 5. Kwee ML, Lindhout D. Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression? Clin Genet 1983;24:200-205.

63. LOGOS Týp Yayýncýlýðý amyoplasia congenita is a subgroup of arthrogryposis multiplex congenita (multiple A case with all the futures of amyoplasia congenita is reported. http://www.logos.com.tr/tr/p_cocuk092003.asp

Yazarlara Bilgi Yayýn Kurulu Son Sayý Arþiv THE JOURNAL OF THE CHILD / EYLÜL 2003 Hipertiroidi, Hiperkortizolizm ve Püberte Prekoks ile Seyreden McCune-Albright Sendromu: Ýki Vaka Sunumu Enver ÞÝMÞEK, Taner YAVUZ, Kenan KOCABAY ÖZET SUMMARY TÜM METÝN Hipertiroidi, Hiperkortizolizm ve Püberta Prekoks ile Seyreden McCune-Albright Sendromu: Ýki Vaka Sunumu McCune-Albright sendromu (MCAS) kemiðin fibrodisplastik lezyonu, düzensiz, sütlü kahve lekeleri þeklinde cilt lez-yonlarý ("café au lait"), hiperfonksiyon ile seyreden bir ve-ya birden fazla endokrinopati ile karakterizedir. Sendrom Ga proteininde aktivasyon mutasyonu sonucu ortaya çýk-maktadýr. Erken puberte, hipertiroidi, Cushing sendromu, akromegali veya jigantizm sýklýkla eþlik eden endokrinopa-tilerdir. Endokrin hiperfonsiyonlar hipotalamo-hipofizer aksdan baðýmsýzdýr. Kliniðimizde MCAS tanýsý konulan iki vaka (14 aylýk erkek sütçocuðu, 7 yaþýnda kýz) sunuldu. Endokrinopati olarak 14 aylýk vakada hipertiroidi ve hi-perkortizolizm, 7 yaþýndaki vakada periferik erken puberte bulgularý saptandý. Çocukluk çaðýnda birden fazla hiperfonksiyon ile seyreden endokrinopatinin eþlik ettiði olgularda ve periferik erken pubertesi olan vakalarda, sütlü kahve lekeleri þeklinde kenarlarý düzensiz cilt lezyonlarý görülürse, ayýrýcý tanýda MCAS'nun da dikkate alýnmasý açýsýndan iki vakanýn sunumu yapýldý.

64. Health/Conditions And Diseases/A -- The Doctors Lounge(TM) amyoplasia congenita@ 88; Amyotrophic Lateral Sclerosis@ 61; Anal Cancer@ 10;Anal Fissures@ 2; Anemia@ 88; Anencephaly@ 15; Aneurysm@ 332 http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/A/index.cgi

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65. Government And Academic Resources On Amyoplasia amyoplasia congenita, Arthromyodysplasia, Congenital. GuerinStern Syndrome, Amyoplasia, Congenita. Asthma Allergy. Allergy and Asthma Network Mothers http://books.mongabay.com/health/conditions/Amyoplasia.html

Amyoplasia Resources U.S. Government resources on Amyoplasia Texas Medical Center News ...or amyoplasia, the most common form of arthrogryposis seen by orthopedic Texas Medical Center News In most cases, the outlook for those with arthrogryposis, particularly with Disabilities Defined ...present in 40% of cases, is a condition called amyoplasia. ... In the typical Penn State Faculty Research Expertise Database (FRED) Amyoplasia Congenita, Arthromyodysplasia, Congenital. Guerin-Stern Syndrome, Contractures Worst with CNS involvement: 50% death in infancy; Best: Amyoplasia Arthrogryposis Amyoplasia, characterized by fatty and fibrous tissue replacement of the limb Pediatric References Amyoplasia, the most common type of Arthrogryposis: the potential for good Baylor College of Medicine ...with special interests in gait disorders of ambulatory children with cerebral Limb anomalies Sturge Weber Syndrome, Epidermolysis Bullosa, Nail Patella Syndrome, VATER Genetic Conditions / Rare Conditions Information Site Anopthalmia; Apert syndrome; Arthrogryposis (amyoplasia); Ataxia (Friedreich Phase I Scholars The full name of my disability is Amyoplasia Arthrogryposis Multiplex Congenita.

66. B-7-‚WDƒ}ƒ‰ƒ`ƒIƒ“iMalathionj Translate this page 3)Lindhout D, Hageman G, amyoplasia congenita-like condition and maternalmalathion exposure. Teratology, 36(1), 7-9, 1987. 4)Kutz FW, Cook BT, http://www.tokyo-eiken.go.jp/edcs/121-75-5.html

Å‰‚̃y[ƒWƒw ‰»ŠwE•¨—“I‚ȏî•ñ ‚Pjƒqƒg‚ÌŒ’N‰e‹¿‚ÉŠÖ˜A‚·‚éî•ñ D Malathion ‚̃XƒvƒŒ[ì‹Æ‚ðs‚Á‚½65Ë‚Ì’j«‚ªCdÇ‚Ì’`”’”A‚𔺂¤–Œ«tÇ‚ð‹N‚±‚µ‚½ D D •Ä‘‚ɏZ‚Þ27801–¼‚Ì”A‚Ì•ªÍ‚ð1976`1980”N‚É‚©‚¯‚čs‚Á‚½D0.5%‚Ì”A‚©‚ç malathion dicarboxylic acid ‚ªC1.1%‚Ì”A‚©‚ç malathion ƒ¿-monocarboxylic acid ‚ªŒŸo‚³‚ꂽ D ‚Qj“à•ª”åŒnE”­¶‰ß’ö‚ɑ΂·‚é‰e‹¿ D ƒAƒ‹ƒrƒmƒ‰ƒbƒg—Y‚É malathion 0.06mg/ƒ‰ƒbƒg/“ú‚ð21“úŠÔŒoŒû“Š—^DŒŒ´’†ƒgƒŠƒˆ[ƒhƒTƒCƒƒjƒ“(T3)‚¨‚æ‚уTƒCƒƒLƒVƒ“ (T4) ‚ÌŒ¸­CTSH •ª”å‚Ì‘‰Á‚ð”F‚ß‚½ D Wistar ƒ‰ƒbƒgŽ“‚É malathion 37mg/ƒ‰ƒbƒg/“ú‚ð2-3“ú‚¨‚«‚É16“úŠÔ• o“à“Š—^D”­î‘OŠú‚©‚ç”­îŠú‚É‚©‚¯‚Ä‚Ì”]“àƒZƒƒgƒjƒ“‚Ì‘‰ÁC”­îŽüŠú‚ð’Ê‚µ‚Ä‚Ì LH ‡¬‚ÌŒ¸­C”­îŠˆ«Šú‚Å‚Ì FSH •úo‘‰ÁC—‘‘ƒŽüŠú‚Ì•sŠˆ«Šú‚É‚¨‚¯‚é LH •úo‚ÌŒ¸­‚ð”F‚ß‚½ D D ‚RjŽÀŒ±“®•¨‚Å‚Ì‘ŸŠíáŠQ«‚ÉŠÖ‚·‚éî•ñ GT3, T4ƒŒƒxƒ‹‚̒ቺ ¸‘ƒˆÞkFƒ‰ƒbƒg@¬‰a@4700ppm@80TŠÔ ŠÌáŠQFƒ‰ƒbƒg@ˆù @1ppm@6ƒ–ŒŽŠÔ táŠQFƒfƒO[ (ƒeƒ“ƒWƒNƒlƒYƒ~‚̈êŽí) @ˆù @200ppm@90“úŠÔ ŒŒŸ÷ƒRƒŠƒ“ƒGƒXƒeƒ‰[ƒ[‚ÌŒ¸­Fƒ‰ƒbƒg@”牺@200mg/kg@6ŽžŠÔŒã tŠÔŽ¿«üˆÛÇFƒ‰ƒbƒg (—Y)@¬‰a@4700ppm@80TŠÔ ‘½”­“®–¬‰ŠFƒ‰ƒbƒg (—Y)@¬‰a@4700ppm@80TŠÔ ‚SjŽîᇔ­¶‚ÉŠÖ‚·‚éî•ñ ‰º‚‘ÌŽîᇁC—‘‘ƒŽîᇁCŠÌŠàFƒ‰ƒbƒg (Ž“)@¬‰a@4700ppm@80TŠÔ bó‘BŽîᇁFƒ‰ƒbƒg (—Y)@¬‰a@8150ppm@80TŠÔ ‰º‚‘ÌŽîᇁC•›tŽîᇁFƒ‰ƒbƒg@¬‰a@4700ppm@80TŠÔ ‚Tj•ÏˆÙŒ´«‚ÉŠÖ‚·‚éî•ñ «õF‘̐«—ò«’vŽ€‘‰ÁFƒVƒ‡ƒEƒWƒ‡ƒEƒoƒG@¬‰a@3.5ƒÊg/l@—c’ŽŠú

67. ForAbby.com - Arthrogryposis Multiplex Congenita - Amyoplasia A site dedicated to our daughter Abby whom was born with Arthrogryposis MultiplexCongenita. http://www.forabby.com/

Welcome to ForAbby.Com. This site is dedicated to our beautiful daughter Abigail Marie. Abby is a typical 3 year old girl with lots of energy and determination. She has always been a strong little girl and continues to show us how determined she is to persevere. She may have weak muscles but she has a strong heart! Abigail has a rare muscle disease called Amyoplasia a form of Arthrogryposis Multiplex Congenita. This site has been up for a little over 2 years now....and I have yet to put up information on Arthrogryposis and how it affects our little girl. I know a lot of visitors come here to research this disease...so I will try and provide as much information as possible. If you use any of this for research projects or presentations please give credit where credit is due. Also if you are using specifics about our daughter please ask us before using her info or pictures in your reports. Arthrogryposis Multiplex Congenita and Amyoplasia Arthrogryposis = curved joints Multiplex = multiple Congenita = evident at birth A = absent myo = muscle plasia = development Arthrogryposis is a rare muscle condition that occurs in approximately 1 in 3000 births. The most common form of Arthrogryposis Multiplex Congenita is Amyoplasia (40% of AMC cases or 1 in 10,000 births). Causes are varied including lack of intrauterine movement - which is suspected in our case. Multiple joint contracture can occur in all limbs but some may be more affected in the upper or lower extremities. Some cases are more severe than others including those that involve the internal organs. Treatment usually occurs soon after birth through splinting, casting, therapy and in some cases surgery. Intellectually, AMC children develop normally and in Abby's case she is a few months behind in her gross and fine motor skills and has a 4-6 month delay in speech.

68. Journal Of Pediatric Orthopaedics B - UserLogin Eight patients with arthrogryposis multiplex congenita (amyoplasia type) Part 1 amyoplasia a common, sporadic condition with congenital contractures. http://www.jpo-b.com/pt/re/jpedorthob/fulltext.01202412-200505000-00015.htm

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69. Journal Of Pediatric Orthopaedics B - Abstract: Volume 14(3) May 2005 P 219-224 Eight patients with arthrogryposis multiplex congenita (amyoplasia type) (11knees) with knee hyperextension deformity underwent quadricepsplasty and were http://www.jpo-b.com/pt/re/jpedorthob/abstract.01202412-200505000-00015.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive Quadricepsplasty in arthrogryposis... ARTICLE LINKS: Fulltext PDF (237 K) Permissions Quadricepsplasty in arthrogryposis (amyoplasia): long-term follow-up. Journal of Pediatric Orthopaedics B. 14(3):219-224, May 2005. Fucs, Patricia M.M.B.; Svartman, Celso; Cesar de Assumpcao, Rodrigo Montezuma; Verde, Saulo Rabelo Lima Abstract: Eight patients with arthrogryposis multiplex congenita (amyoplasia type) (11 knees) with knee hyperextension deformity underwent quadricepsplasty and were analyzed during an average follow-up period of 11 years and 2 months. The results were clinically analyzed based on gait pattern, range of movement, and orthotic requirements. Joint congruency was evaluated by radiography according to the Leveuf Pais classification. A satisfactory result was the correction of the deformity, articular congruency, sufficient range of movement, adequate gait pattern and no need for orthosis. A satisfactory outcome occurred in five of the eight patients (eight knees). We considered an unsatisfactory result when any of these conditions occurred. Our experience demonstrated that the quadricepsplasty corrected the hyperextension deformity of the knee joint, improved function, gait pattern, and maintained the muscle power of the quadriceps. Subscribe to RSS feed utrdc-pt02 Release 4.0

70. Arthrogryposis was two days old with arthrogryposis multiplex congenita, or amyoplasia, Of all children with amyoplasia, the most common form of arthrogryposis, 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?

71. Texas Medical Center News she was 2 days old with arthrogryposis multiplex congenita, or amyoplasia, Of all children with amyoplasia, the most common form of arthrogryposis, http://www.tmc.edu/tmcnews/09_01_99/page_04.html

Vol. 21, No. 16 September 1, 1999 Help for Patients with Arthrogryposis Straight Talk About Curved Joints by RONDA WENDLER Shriners Hospital for Children 16-year-old Jennifer Weaver, an arthrogryosis patient at Shriners, 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?

72. Ortho Hyperguide. Login Page and congenital vertical talus, neither of which is present in amyoplasia. Patients who present with amyoplasia have certain characteristic criteria. http://www.ortho.hyperguides.com/Tutorials/pediatric_ort/Arthrogryposis/tutorial

Welcome to the ORTHOPEDICS Hyperguide TM The ORTHOPEDICS Hyperguide TM is a state-of-the-art online educational program, designed for health care professionals worldwide. It features tutorials online lectures , and test questions in the following areas: Adult Orthopedics, Basic Science, Foot and Ankle, Hand, Orthobiologics and Pharmacologics, Pediatric Orthopedics, Spine, Sports Medicine, Trauma, and Tumor. If you have a User ID and Password please enter them in the fields above and click "Log in." If you would like to access the ORTHOPEDICS Hyperguide TM please click here: Tutorials provide you with an overview of important topics and focus on areas such as clinical and radiographic features, diagnosis, risk factors, evaluation, treatment options, and patient outcomes. Throughout each tutorial, you will be able to access images, including clinical photographs, radiographs, and magnetic resonance images. If you would like additional information on a specific topic, bibliographies are included at the conclusion of each tutorial. Online lectures simulate the lecture experience. Experts in the orthopedic community provide lectures in their respective specialty areas. The slides automatically advance along with the audio, and a transcript of the lecture is shown below the slides. Printable transcripts of the lectures are also available.

73. List Of Diseases Starting With A: Information From Answers.com Amathophobia; Amaurosis congenita of Leber, type 1; Amaurosis congenita of Leber, amyoplasia mandibulofacial dysostosis; amyoplasia; Amyotonia congenita http://www.answers.com/topic/list-of-diseases-starting-with-a

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping List of diseases starting with A Wikipedia List of diseases starting with A A listing of diseases A B C D E ... Z Aa-Ab 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 Ac Aca-Acc Acalvaria Acanthocheilonemiasis Acanthocytosis chorea Acanthocytosis Acanthosis nigricans muscle cramps acral enlargement Acarophobia Acatalasemia Accessory deep peroneal nerve Accessory Navicular bone Accessory pancreas Ach-Ack Achalasia alacrimia syndrome Achalasia microcephaly Achalasia, familial esophageal

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

75. Core Curriculum - POSNA Describe clinical features of arthrogryposis multiplex congenita amyoplasia,the most common type of arthrogryposis the potential for good outcome. http://www.posna.org/index?service=page/coreCurriculum&article=arthrogryposis.ht

76. Encyclopedia: List Of Diseases Familial; Amyloidosis; Amylopectinosis; amyoplasia mandibulofacial dysostosis;amyoplasia; Amyotonia congenita; Amyotrophic lateral sclerosis http://www.nationmaster.com/encyclopedia/List-of-diseases

Supporter Benefits Signup Login Sources ... Pies Related Articles People who viewed "List of diseases" also viewed: List of diseases starting with B List of diseases starting with W List of diseases starting with F List of diseases starting with S ... List of diseases starting with D What's new? Our next offering Latest newsletter Student area Lesson plans Recent Updates Charles L. Perkins Cazenovia (village), New York Cat Carry On ... More Recent Articles Top Graphs Richest Most Murderous Most Taxed Most Populous ... More Stats Encyclopedia: List of diseases Updated 209 days 6 hours 58 minutes ago. Other descriptions of List of diseases A listing of diseases A B C D E ... Z Contents 1 Aa-Ab 2 Ac 2.1 Aca-Acc 2.2 Ach-Ack ... 15 Au-Az Aa-Ab 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 Ac Aca-Acc Acalvaria Acanthocheilonemiasis Acanthocytosis chorea Acanthocytosis Acanthosis nigricans muscle cramps acral enlargement Acarophobia Acatalasemia Accessory deep peroneal nerve Accessory Navicular bone Accessory pancreas Ach-Ack Achalasia alacrimia syndrome Achalasia microcephaly

77. List Of Diseases Starting With A -- Facts, Info, And Encyclopedia Article amyoplasia mandibulofacial dysostosis amyoplasia Amyotonia congenita (Thickeningof tissue in the motor tracts of the lateral columns and anterior horns of http://www.absoluteastronomy.com/encyclopedia/l/li/list_of_diseases_starting_wit

List of diseases starting with A [Categories: Lists of diseases] A listing of (An impairment of health or a condition of abnormal functioning) disease s. A (The 2nd letter of the Roman alphabet) B (The 3rd letter of the Roman alphabet) C (The 4th letter of the Roman alphabet) D (The 5th letter of the Roman alphabet) E (The 6th letter of the Roman alphabet) F (The 7th letter of the Roman alphabet) G (The 8th letter of the Roman alphabet) H (The 9th letter of the Roman alphabet) I (The 10th letter of the Roman alphabet) J (The 11th letter of the Roman alphabet) K (The 12th letter of the Roman alphabet) L (The 13th letter of the Roman alphabet) M (The 14th letter of the Roman alphabet) N (The 15th letter of the Roman alphabet) O (The 16th letter of the Roman alphabet) P (The 17th letter of the Roman alphabet) Q (The 18th letter of the Roman alphabet) R (The 19th letter of the Roman alphabet) S (The 20th letter of the Roman alphabet) T (The 21st letter of the Roman alphabet) U (The 22nd letter of the Roman alphabet) V (The 23rd letter of the Roman alphabet) W (The 24th letter of the Roman alphabet) X (The 25th letter of the Roman alphabet) Y (The 26th letter of the Roman alphabet) Z Aa-Ab (Click link for more info and facts about Aagenaes syndrome) Aagenaes syndrome Aarskog Ose Pande syndrome (Click link for more info and facts about Aarskog syndrome) Aarskog syndrome Aase Smith syndrome (Click link for more info and facts about Aase syndrome) Aase syndrome ABCD syndrome Abdallat Davis Farrage syndrome (An aneurysm of the abdominal aorta associated with old age and hypertension)

78. List Of Diseases Starting With A - Enpsychlopedia Familial Amyloidosis Amylopectinosis amyoplasia mandibulofacial dysostosis amyoplasia Amyotonia congenita Amyotrophic lateral sclerosis http://psychcentral.com/psypsych/List_of_diseases

home resource directory disorders quizzes ... support forums Advertisement ( List of diseases starting with A (Redirected from List of diseases A listing of diseases A B C D E ... Z Contents showTocToggle("show","hide") 1 Aa-Ab 2 Ac 2.1 Aca-Acc 2.2 Ach-Ack ... edit Aa-Ab Aagenaes syndrome Aarskog Ose Pande syndrome Aarskog syndrome Aase Smith syndrome ... edit Ac edit Aca-Acc Acalvaria Acanthocheilonemiasis Acanthocytosis chorea Acanthocytosis ... edit Ach-Ack Achalasia alacrimia syndrome Achalasia microcephaly Achalasia, familial esophageal Achalasia ... edit Acn-Acq Acne rosacea Acne Acoustic neuroma Acoustic schwannomas ... edit Acr edit Acra Acral dysostosis dyserythropoiesis Acral renal mandibular syndrome edit Acro Acro coxo mesomelic dysplasia Acro fronto facio nasal dysostosis edit Acroc-Acrok Acrocallosal syndrome, Schinzel type Acrocephalopolydactyly Acrocephalosyndactyly Jackson Weiss type Acrocephaly pulmonary stenosis mental retardation ... edit Acrom-Acros Acromegaloid changes cutis verticis gyrata corneal Acromegaloid facial appearance syndrome Acromegaloid hypertrichosis syndrome Acromegaly ... edit Act ACTH deficiency ACTH resistance Actinomycetales infection Activated protein C resistance ... edit Acu edit Acut edit Acuta Acutane embryopathy edit Acute edit Acute a-Acute l Acute articular rheumatism Acute erythroblastic leukemia Acute febrile neutrophilic dermatosis Acute idiopathic polyneuritis ... edit Acute m-Acute r Acute megakaryoblastic leukemia Acute monoblastic leukemia Acute mountain sickness Acute myeloblastic leukemia type 1 ... Acute myeloid leukemia, secondary

79. Acid Maltase Deficiency amyoplasia, congenita. Asthma Allergy. Allergy and Asthma Network Mothers ofAsthmatics. 2751 Prosperity Ave., Ste. 150. Fairfax, VA 220314397 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

80. NEUROMUSCULAR DISORDERS Arthrogryposis Multiplex congenita, amyoplasia This is a non progressive disorderwith multiple, congenitally rigid joints. It is caused by any of several 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.

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