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         Riley-day Syndrome:     more detail

41. Health/Conditions And Diseases/Neurological Disorders/Autonomic Nervous System/F
Also known as rileyday syndrome. url www.fdvillage.org; FD Home Page A descriptionof familial dysautonomia with a look at he clinical symptoms,
http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Neurological_
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  • report abuse/spam url: report-abuse.dmoz.org/?cat=Health/Conditions_and_D... The CaF Directory An article about familial dysautonomia and its inheritance patterns. Also information about a support group for those living in the UK. url: www.cafamily.org.uk/Direct/f17.html Cure-FD Foundation Peruse the latest news on the work being done in finding a cure as well as finding information on Familial Dysautonomia. url: curefd.org Dysautonomia Foundation Familial dysautonomia, press releases, information on summer camps for kids and adults, details about the organization and FD itself. url: www.familialdysautonomia.org Dysautonomia Treatment and Evaluation Center NYU School of Medicine Department of Pediatrics and Department of Neurology offers genetic information and counseling, patient care and staff information. url: www.med.nyu.edu/fd/index.html
  • 42. RILEY-DAY SYNDROME Definition
    Home/R/ri/rileyday syndrome. Medical Dictionary Search Engine. September isNational Mesothelioma awareness month! Mesothelioma is hard to detect,
    http://www.books.md/R/dic/rileydaysyndrome.php
    Home R ri /RILEY-DAY SYNDROME
    Medical Dictionary Search Engine September is National Mesothelioma awareness month! Mesothelioma is hard to detect, easily mis-diagnosed, and always fatal. Have your doctor check you for Mesothelioma or Pleural Mesothelioma today! Browse Dictionary by alphabet A B C D ... Z
    September is National Mesothelioma awareness month! Mesothelioma is hard to detect, easily mis-diagnosed, and always fatal. Have your doctor check you for Mesothelioma or Pleural Mesothelioma today! Asbestos is a mineral widely used in the past because of its resistance to fire and heat. Loose asbestos fibers can lodge in the surrounding tissues of the lungs and cancerous tissues can develop into Pleural Mesothelioma. The disease may be treated with drugs like Alimta or Cisplatin, but it is essential for everyone to know the symptoma and get tested for Mesothelioma Home

    43. Healthfinder® - Riley-Day Syndrome
    Carefully selected government and nonprofit health information on rileyday syndrome.
    http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=753&show=1

    44. BIND - The Biomolecular Interaction Network
    FD; IKBKAP; dysautonomia (rileyday syndrome; DKFZp781H1425; DYS; dysautonomia (Riley-Daysyndrome, hereditary sensory autonomic neuropathy type III)
    http://bind.ca/Action?idsearch=gi:38569394

    45. Dysautonomia Familial,FD,Hereditary Sensory And Autonomic
    rileyday syndrome. Familial Dysautonomia is a rare genetic disorder of theautonomic nervous system (ANS) that primarily affects people of Eastern European
    http://www.icomm.ca/geneinfo/dysaut.htm

    46. The Motor-Sensory Unit System
    rileyday syndrome or familial dysautonomia may produce neonatal hypotonia. Sural biopsy in patients with riley-day syndrome shows a reduction or
    http://pediatricneuro.com/alfonso/pg135.htm
    MainMenu Back Next Index
    Neuronal-Axonal Disease Not Associated with Werdnig-Hoffmann Disease
    Neuronal-axonal disease not associated with Werdnig-Hoffmann disease is a rare condition that primarly involves the axons. Neuronal-axonal disease not associated with Werdnig-Hoffmann disease refers to a group of peripheral neuropathies in which the axon is the primary structure involved. Nerve conduction is normal or only moderately slow. It is diagnosed by sural nerve biopsy. The biopsy shows sphered bodies in the axons, particularly in the presynaptic region. It is important to diagnose this entity because neonates with this disorder may not deteriorate and may even improve with time. The disease has a sporadic or autosomal-dominant inheritance. Giant Axonal Neuropathy
    Giant axonal neuropathy is a rare condition that involves the central and peripheral nervous systems. It should be suspected when the patient has tightly curled, kinky, poorly pigmented scalp hair. Motor and sensory nerve conduction velocity may not be decreased. The diagnosis is established by finding greatly enlarged axons filled with disarrayed neurofilaments in sural nerve biopsy. The cause is probably an error of metabolism affecting the formation of neurofilaments. Infantile Porphyria
    Infantile porphyria may produce neonatal hypotonia. The clinical course is characterized by recurrent polyneuropathy. Nerve conduction velocity is normal. The characteristic findings are increased urine delta-aminolevulinic acid and coproporphyrin levels and decreased erythrocyte aminolevulinic acid synthetase activity.

    47. Welcome To Spirit Magazine
    Our baby had rileyday syndrome, or as it is now called, Familial Dysautonomia,or FD. He looked at us and stammered, barely audibly, “Your doctor will call
    http://www.spiritmag.org/v3n1/fd_ourstory.html
    Spring 2005 Vol 3 / No. 3 Yedei Chesed is a contract agency certified by the New York State Office of Mental Retardation and Developmental Disabilities. By Lana Steiner The diagnosis came on Shabbos. So many minutiae have been forgotten in the eight intervening years, but every single detail of that day is sharp in my memory, and every facet of the previous day has been conjured up to fit all the pieces together.
    Our first child, a daughter, came after a fairly normal pregnancy; no major causes for alarm. Doctors ordered six weeks of bed rest for low amniotic fluid, but the baby was fine. Then one morning, just after my husband, David, left for work, my water broke. After twelve hours of labor, at 11:21 p.m. on a cool Friday night in March, our beautiful redheaded daughter was born.
    And she really was a beautiful baby. Her APGAR scores were normal; we were in seventh heaven. Since it was Shabbos, we had the luxury of getting to know our baby without any intrusions. We were beginning to form our new little family.

    48. Brain Foundation - Dysautonomia
    dysautonomia and familial dysautonomia and rileyday syndrome. FamilialDysautonomia (also known as riley-day syndrome) is a rare genetic disorder that
    http://www.brainaustralia.org.au/AZ_of_Brain_Disorders/dysautonomia
    Home About Us The Brain Healthy Brain ... Site Map DHTML_MENU_rel_path = '/squizlib/dhtml_menu/images/';
    Dysautonomia
    (Familial Dysautonomia, Riley-Day Syndrome)
    Description
    Familial Dysautonomia (also known as Riley-Day Syndrome) is a rare genetic disorder that affects the sensory and autonomic nerve system. It is found primarily in children of Eastern European Jewish background (Ashkenazi Jews) who have inherited two recessive genes (i.e. one from each parent). People born with this disorder have a reduced number of nerve fibres; as a result, they have reduced sensations of pain, touch, temperature and taste. In addition, they are unable to produce overflow tears, have impaired motor coordination, and have difficulty with sucking and swallowing. This leads to repeated vomiting, and frequent lung infections that are brought about by gastrointestinal fluids entering the lungs. Other problems that may occur include excessive sweating, seizures, scoliosis and delayed puberty in girls.
    Treatment
    While there is no cure for this genetic disorder, medical care is directed at relieving the symptoms it causes. For example, a feeding tube inserted into the stomach can assist in feeding, and prevent fluids etc. from entering the lungs, while drugs are prescribed to prevent vomiting and seizures, eye drops lubricate dry eyes, and surgery can correct scoliosis.
    Prognosis
    With improved medical care, the life expectancy of people with Dysautonomia is increasing, and about 50 per cent live to the age of 30.

    49. Beliefnet: Health And Healing
    Advanced heart failure; Addison’s disease; Diabetes; Pernicious anemia;Amyloidosis; GuillainBarre syndrome; riley-day syndrome; Shy-Drager syndrome
    http://www.beliefnet.com/healthandhealing/getcontent.aspx?cid= 34315

    50. Search By Disease
    rileyday syndrome. 110, riley-day syndrome. 111, Riley-Smith syndrome. 112,Robinow syndrome, autosomal recessive. 113, Rod monochromacy 2 (RMCH2)
    http://www.eddnal.com/directory/disease.php?letter=R&page=8

    51. Entrez PubMed
    Familial dysautonomia, or rileyday syndrome, is a hereditary disturbance in theautonomic and perip
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7

    52. Entrez PubMed
    Nonspinal orthopaedic problems in familial dysautonomia (rileyday syndrome).Laplaza FJ, Turajane T, Axelrod FB, Burke SW.
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

    53. Orthostatic Hypotension - Swedish Medical Center, Seattle, Washington
    Advanced heart failure; Addisons disease; Diabetes; Pernicious anemia;Amyloidosis; GuillainBarre syndrome; riley-day syndrome; Shy-Drager syndrome
    http://www.swedish.org/14456.cfm
    PDF Version Search Send-to-Friend Health Library Home ... Conditions InBrief
    Orthostatic Hypotension
    (Postural Hypotension)
    by Diane Voyatzis, RD Definition Causes Risk Factors ... Prevention
    Definition
    Orthostatic hypotension is a condition of abnormal blood pressure regulation upon standing. The blood pressure dramatically decreases (more than 20/10 mm Hg) when rising from a lying down or sitting position to a standing position. Measuring of Blood Pressure www.nucleusinc.com
    Causes
    Orthostatic hypotension has several causes.
    • Hypovolemia is the most common cause. It may be due to:
      • Excessive use of loop diuretic medications (furosemide, bumetanide, ethacrynic acid) Vasodilator medications (nitrate preparations, Ca blockers, or ACE inhibitors) Dehydration Prolonged bed rest Addisons disease (with inadequate salt intake)
      Impaired autonomic (nerve) reflex due to certain diseases: Decreased heart muscle contractility or vascular responsiveness Certain drugs:
      • Monoamine oxidase inhibitors (MAO inhibitors) (isocarboxazid, phenelzine, tranylcypromine)

    54. Blackwell Synergy - Cookie Absent
    Familial dysautonomia (rileyday syndrome) may be associated with epilepsy.Epilepsia 2003;44 472. Epilepsia Volume 45 Issue 11 Page 1461 - November 2004
    http://www.blackwell-synergy.com/doi/abs/10.1111/j.0013-9580.2004.54403.x
     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.

    55. Journal Of Pediatric Orthopaedics - UserLogin
    Familial dysautonomia (rileyday syndrome) is an autosomal recessive disorder Unusual case of charcot joints in early adolescence (riley-day syndrome).
    http://www.pedorthopaedics.com/pt/re/jpedortho/fulltext.00004694-200103000-00019
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    56. Journal Of Pediatric Orthopaedics - Abstract: Volume 21(2) March/April 2001 P 22
    Nonspinal Orthopaedic Problems in Familial Dysautonomia (rileyday syndrome).Journal of Pediatric Orthopedics. 21(2)229-232, March/April 2001.
    http://www.pedorthopaedics.com/pt/re/jpedortho/abstract.00004694-200103000-00019
    LWWOnline LOGIN eALERTS REGISTER ... Archive Nonspinal Orthopaedic Problems... ARTICLE LINKS:
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    PDF (285 K) Permissions Nonspinal Orthopaedic Problems in Familial Dysautonomia (Riley-Day Syndrome).
    Journal of Pediatric Orthopedics. 21(2):229-232, March/April 2001.
    Laplaza, F. Javier M.D.; Turajane, Thana M.D. *; Axelrod, Felicia B. M.D. +; Burke, Stephen W. M.D. Abstract:
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    57. List Of Diseases Starting With R: Information From Answers.com
    Rambam Hasharon syndrome; Rambaud Galian syndrome; Ramer Ladda syndrome rileyday syndrome; Ringed hair disease; Ringworm; Rivera Perez Salas syndrome
    http://www.answers.com/topic/list-of-diseases-starting-with-r
    showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Or search: - The Web - Images - News - Blogs - Shopping List of diseases starting with R Wikipedia List of diseases starting with R A list of diseases in the English wikipedia. A B C D ... Q R S T U V ... Z
    Ra
    Rab-Rai
    • Rabies Rabson-Mendenhall syndrome Radial defect Robin sequence Radial hypoplasia, triphalangeal thumbs and hypospadias Radial ray agenesis Radial ray hypoplasia choanal atresia Radiation induced angiosarcoma of the breast Radiation induced meningioma Radiation leukemia Radiation related neoplasm /cancer Radiation syndromes Radiation-Induced Brachial Plexopathy Radiculomegaly of canine teeth congenital cataract Radio digito facial dysplasia Radio renal syndrome Radiophobia Radioulnar synostosis mental retardation hypotonia Radioulnar synostosis retinal pigment abnormalities Radio-ulnar synostosis type 1 Radio-ulnar synostosis type 2 Radius absent anogenital anomalies Raine syndrome
    Ram-Ray
    • Rambam Hasharon syndrome Rambaud Galian syndrome Ramer Ladda syndrome Ramon Syndrome Ramos Arroyo Clark syndrome Ramsay Hunt paralysis syndrome Rapadilino syndrome Rapp-Hodgkin syndrome Rasmussen encephalitis Rasmussen Johnsen Thomsen syndrome Rasmussen subacute encephalitis Ray Peterson Scott syndrome Raynaud's disease/phenomenon Rayner Lampert Rennert syndrome
    Re
    Rea-Reg
    • Reactive airway disease Reactive arthritis Reactive attachment disorder of early childhood Reactive attachment disorder of infancy Reactive hypoglycemia Reardon Hall Slaney syndrome

    58. Orthostatic Hypotension - Gastonia, North Carolina
    Advanced heart failure; Addison s disease; Diabetes; Pernicious anemia;Amyloidosis; GuillainBarre syndrome; riley-day syndrome; Shy-Drager syndrome
    http://www.caromont.org/12077.cfm
    Print Search Send to a friend
    Be Well
    ... Cancer InDepth
    �Diseases, Conditions and Injuries
    Orthostatic Hypotension
    (Postural Hypotension)
    by Diane Voyatzis, RD Definition Causes Risk Factors ... Organizations
    Definition
    Orthostatic hypotension is a condition of abnormal blood pressure regulation upon standing. The blood pressure dramatically decreases (more than 20/10 mm Hg) when rising from a lying down or sitting position to a standing position. Measuring of Blood Pressure www.nucleusinc.com
    Causes
    Orthostatic hypotension has several causes.
    • Hypovolemia is the most common cause. It may be due to:
      • Excessive use of loop diuretic medications (furosemide, bumetanide, ethacrynic acid) Vasodilator medications (nitrate preparations, Ca blockers, or ACE inhibitors) Dehydration Prolonged bed rest Addison's disease (with inadequate salt intake)
      Impaired autonomic (nerve) reflex due to certain diseases: Decreased heart muscle contractility or vascular responsiveness Certain drugs:
      • Monoamine oxidase inhibitors (MAO inhibitors) (isocarboxazid, phenelzine, tranylcypromine)

    59. Orthostatic Hypotension - WI, Milwaukee WI
    Advanced heart failure; Addison�s disease; Diabetes; Pernicious anemia;Amyloidosis; GuillainBarre syndrome; riley-day syndrome; Shy-Drager syndrome
    http://www.columbia-stmarys.org/13617.cfm
    Print Search Send to a friend Home �Diseases, Conditions and Injuries
    Orthostatic Hypotension
    (Postural Hypotension)
    by Diane Voyatzis, RD Definition Causes Risk Factors ... Organizations
    Definition
    Orthostatic hypotension is a condition of abnormal blood pressure regulation upon standing. The blood pressure dramatically decreases (more than 20/10 mm Hg) when rising from a lying down or sitting position to a standing position. Measuring of Blood Pressure www.nucleusinc.com
    Causes
    Orthostatic hypotension has several causes.
    • Hypovolemia is the most common cause. It may be due to:
      • Excessive use of loop diuretic medications (furosemide, bumetanide, ethacrynic acid) Vasodilator medications (nitrate preparations, Ca blockers, or ACE inhibitors) Dehydration Prolonged bed rest Addison�s disease (with inadequate salt intake)
      Impaired autonomic (nerve) reflex due to certain diseases: Decreased heart muscle contractility or vascular responsiveness Certain drugs:
      • Monoamine oxidase inhibitors (MAO inhibitors) (isocarboxazid, phenelzine, tranylcypromine)

    60. EMedicine - Cyclic Vomiting Syndrome : Article By Shikha Sundaram, MD
    One extreme example, rileyday syndrome (familial dysautonomia), manifests asboth autonomic Familial dysautonomia (riley-day syndrome) Renal disorders
    http://www.emedicine.com/ped/topic2910.htm
    (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Gastroenterology
    Cyclic Vomiting Syndrome
    Last Updated: August 10, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: CVS, vomit, emesis, migraine, syndrome of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes, MELAS syndrome, abdominal migraine AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
    Author: Shikha Sundaram, MD , Fellow, Department of Gastroenterology, Hepatology and Nutrition, Children's Memorial Hospital of Chicago and Northwestern University Coauthor(s): B UK Li, MD , Director, Division of Gastroenterology, Hepatology and Nutrition, Children's Memorial Hospital of Chicago; Professor, Department of Pediatrics, Northwestern University Shikha Sundaram, MD, is a member of the following medical societies: American Academy of Pediatrics , and American Medical Association Editor(s): Jayant Deodhar, MD

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