21. Riley-Day Syndrome - Overview rileyday syndrome. Alternative names Familial dysautonomia. DefinitionAn inherited disorder that affects sensory and autonomic http://www.wfubmc.edu/besthealth/ency/article/001387.htm

Disease Injury Nutrition Poison ... Prevention Riley-Day syndrome Alternative names: Familial dysautonomia Definition: An inherited disorder that affects sensory and autonomic function in many organ systems. Causes, incidence, and risk factors: Riley-Day syndrome is inherited as an autosomal recessive trait that is found predominantly in the European Jewish population (Ashkenazi Jews). Infants with this condition have feeding problems and develop pneumonia caused by inhalation of their formula and food. Episodic vomiting and sweating spells begin following infancy. Young children also have breath-holding spells that produce unconsciousness Insensitivity to pain is a hallmark of Riley-Day syndrome and leads to unnoticed injuries or injuries that might not have occurred had the child sensed discomfort. Children do not feel the normal sensations that generally warn of impending injury such as drying of the eyes, pressure over pressure points, and chronic rubbing and chaffing. Seizures may occur in almost 50% of affected children. They have postural hypotension or hypertensive crises. Temperature regulation may be deficient.

22. Riley-Day Syndrome - Treatment rileyday syndrome. Call your health care provider if you have a family historyof riley-day syndrome and are planning to have a child or expecting a child. http://www.wfubmc.edu/besthealth/ency/article/001387trt.htm

Disease Injury Nutrition Poison ... Prevention Riley-Day syndrome Alternative names: Familial dysautonomia Treatment: Protection from injury is critical. Problems are treated as they occur, including treatment of aspiration pneumonia , anticonvulsant therapy if seizures are present, and liquid tears and bethanechol to prevent drying of eyes. Antiemetics may be used to control vomiting Expectations (prognosis): Most people with this syndrome die in childhood. Complications: Charcot joints from injury increased incidence of diabetes mellitus Calling your health care provider: Call your health care provider if you have a family history of Riley-Day syndrome and are planning to have a child or expecting a child. If you are unsure of your family history but belong to a high risk population it may be helpful to consult a genetic counselor. Acquired On: 1/1/97 Acquired From: Mosby Publishing Company The information provided herein should not be used for diagnosis or treatment of any medical condition. It is provided for your general information and is not a substitute for medical care or supervised medical treatment. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. adam.com is a founding member of Hi-Ethics (http://www.hiethics.com)

23. Ask Jeeves: Search Results For "Riley Day Syndrome" Popular Web Sites for Riley Day Syndrome . Search Results 1 10 Rankedby Popularity, Next . 1. riley-day syndrome a CHORUS notecard http://webster.directhit.com/webster/search.aspx?qry=Riley Day Syndrome

24. Ask Jeeves: Search Results For "Familial Dysautonomia Disease" Dysautonomia Genetics Education and Counseling Program Familial Dysautonomia brochurehttp//www.pitt.edu/~edugene/FD.html 4. rileyday syndrome a CHORUS http://webster.directhit.com/webster/search.aspx?qry=Familial Dysautonomia Disea

25. Riley-Day Syndrome - General Practice Notebook Practice Notebook. rileyday syndrome. Familial dysautonomia is a raresyndrome caused by an inborn error of catecholamine metabolism. It http://www.gpnotebook.co.uk/cache/-852164570.htm

Riley-Day syndrome Familial dysautonomia is a rare syndrome caused by an inborn error of catecholamine metabolism. It is inherited in an autosomal recessive manner, mainly in Jews. Most sufferers die from respiratory infection or uraemia in early childhood. Click here for more information...

26. Riley Day Syndrome riley day syndrome a CHORUS notecard document about rileyday syndrome Riley-Daysyndrome. familial dysautonomia. home Disease R riley-day syndrome. http://www.calgaryhabitat.com/travel-trip-planning-vacation.htm

27. Health Library Find Information On Riley-Day Syndrome At rileyday syndrome. Definition A person who lives into their 40s is old for a Riley-Daysyndrome patient. Half of patients do not survive past 20 years of age. http://www.mercksource.com/pp/us/cns/cns_hl_adam.jspzQzpgzEzzSzppdocszSzuszSzcns

28. ENLmedical.com: Conditions And Concerns: Medical Encyclopedia: Riley-Day Syndrom Table of content. rileyday syndrome. Prevention Genetic counseling is recommendedfor prospective parents if there is a family history of riley-day syndrome. http://www.enlmedical.com/article/001387.htm

Medical Dictionary Naturapathic Glossary Aphrodisiacs Immune System ... Table of content Riley-Day syndrome Causes and Risks: Riley-Day syndrome is inherited as an autosomal recessive trait that is found predominantly in the European Jewish population (Ashkenazi Jews). Infants with this condition have feeding problems and develop pneumonia caused by inhalation of their formula and food. Episodic vomiting and sweating spells begin following infancy. Young children also have breath-holding spells that produce unconsciousness Insensitivity to pain is a hallmark of Riley-Day syndrome and leads to unnoticed injuries or injuries that might not have occurred had the child sensed discomfort. Children do not feel the normal sensations that generally warn of impending injury such as drying of the eyes, pressure over pressure points, and chronic rubbing and chaffing. Seizures may occur in almost 50% of affected children. They have postural hypotension or hypertensive crises. Temperature regulation may be deficient. Prevention: Genetic counseling is recommended for prospective parents if there is a family history of Riley-Day syndrome.

29. Health Ency.: Disease: Riley-Day Syndrome Ency. home Disease R rileyday syndrome. riley-day syndrome. A personwho lives into their 40s is old for a riley-day syndrome patient. http://www.accessatlanta.com/shared/health/adam/ency/article/001387trt.html

SEARCH: The Web Yellow Pages HOME AJC.COM Illustrated Health Encyclopedia Important notice Ency. home Disease R Riley-Day syndrome Overview Symptoms Treatment Prevention Alternative names: Familial dysautonomia; Hereditary sensory and autonomic neuropathy - type III Treatment Protection from injury is critical. Problems are treated as they occur, including treatment of aspiration pneumonia , anticonvulsant therapy if seizures are present, and liquid tears and bethanechol to prevent drying of eyes. Antiemetics may be used to control vomiting Prognosis Most people with this syndrome do not live to normal life expectancy. A person who lives into their 40s is old for a Riley-Day syndrome patient. Half of patients do not survive past 20 years of age. Complications Charcot joints from repeated injury increased incidence of diabetes mellitus phobias and emotional diorders Call Your Health Care Provider If: Call your health care provider if you have a family history of Riley-Day syndrome and are planning to have a child or expecting a child. If you are unsure of your family history but belong to a high risk population it may be helpful to consult a genetic counselor. Ency. home

30. Health Content Encyclopedia Article Riley-Day Syndrome rileyday syndrome A person who lives into their 40s is old for a Riley-Daysyndrome patient. Half of patients do not survive past 20 years of age. http://www.centralbap.com/adamcontent/ency/article/001387.asp

31. Database Search Results Database Search Results. Searched keywords for rileyday syndrome.Dysautonomia Treatment and Evaluation Center. NHIC Home Page http://www.health.gov/nhic/NHICScripts/Hitlist.cfm?Keyword=Riley-Day Syndrome

32. Health Information Resources: Keyword Listing Rhinitis; rileyday syndrome; Risk Reduction; Rubella; Rubinstein-Taybi Syndrome;Runaway Youth; Running; Rural Health; Russell-Silver Syndrome. NHIC Home Page http://www.health.gov/nhic/NHICScripts/AlphaKey.cfm?Alpha=R

33. Riley-Day Syndrome rileyday syndrome. Prevention Genetic counseling is recommended for prospectiveparents if there is a family history of riley-day syndrome. http://www.rwjuhh.net/Atoz/encyclopedia/article/001387.asp

For a complete list of hospital classes and events, click here to connect to HealthConnection Online Medical Encyclopedia Encyclopedia Disease R -> Riley-Day syndrome Riley-Day syndrome Alternate Names: Familial dysautonomia; Hereditary sensory and autonomic neuropathy - type III Causes and Risks: Riley-Day syndrome is inherited as an autosomal recessive trait that is found predominantly in the European Jewish population (Ashkenazi Jews). The disease is caused by mutation of the IKBKAP gene on chromosome 9. It is not rare in Ashkenazi Jews where the incidence is estimated to be 1 in 3700 people. Infants with this condition have feeding problems and develop pneumonia caused by inhalation of their formula and food. Episodic vomiting and sweating spells begin following infancy. Young children also have breath-holding spells that produce unconsciousness Insensitivity to pain is a hallmark of Riley-Day syndrome and leads to unnoticed injuries or injuries that might not have occurred had the child sensed discomfort. Children do not feel the normal sensations that generally warn of impending injury such as drying of the eyes, pressure over pressure points, and chronic rubbing and chaffing.

34. Home Family Resources How Can I Help? Research Finance Dysautonomic face. Familial dysautonomia (rileyday syndrome). Familialdysautonomia (riley-day syndrome). riley-day syndrome. http://www.fdvillage.org/search_title.asp

Home Family Resources How Can I Help? Research ... Contact Us All Current Titles Listed Please Click A Title To View Details [A case of acute idiopathic pandysautonomia]. [Anesthesia and intensive therapy in autonomic dysfunction]. [Autonomic neuropathy of the peripheral nerves]. [Clinical reflections of familial dysautonomia]. ... Use of vaccinia virus vectors to study protein processing in human disease. Normal nerve growth factor processing and secretion in cultured fibroblasts from patients with familial dysautonomia. © 2000 FD Village

35. Roche Lexikon Medizin (4. Aufl.) - Riley*-Day* Syndrom engl. riley-day syndrome; familial dysautonomia. eine http://www.gesundheit.de/roche/ro32500/r33563.html

Riley*-Day* Syndrom engl.: Riley-Day syndrome; familial dysautonomia Verwandte Themen Dysautonomie Dysfunctio, Dysfunktion Neuropathie

36. Riley-Day Syndrome Home Medical Reference Encyclopedia (English)Toggle English / Spanish rileyday syndrome. http://www.northarundel.com/ency/article/001387.htm

Disease Nutrition Surgery Symptoms Injury ... Z Related Programs at North Arundel Hospital Maryland Vascular Center Home Medical Reference Encyclopedia (English) Toggle English Spanish Riley-Day syndrome Overview Symptoms Treatment Prevention Definition: An inherited disorder that affects sensory and autonomic nerve function in many body parts/systems. Alternative Names: Familial dysautonomia; Hereditary sensory and autonomic neuropathy - type III Causes, incidence, and risk factors: Riley-Day syndrome is inherited as an autosomal recessive trait that is found predominantly in the European Jewish population (Ashkenazi Jews). The disease is caused by mutation of the IKBKAP gene on chromosome 9. It is not rare in Ashkenazi Jews where the incidence is estimated to be 1 in 3700 people. Infants with this condition have feeding problems and develop pneumonia caused by inhalation of their formula and food. Episodic vomiting and sweating spells begin following infancy. Young children also have breath-holding spells that produce unconsciousness Insensitivity to pain is a hallmark of Riley-Day syndrome and leads to unnoticed injuries or injuries that might not have occurred had the child sensed discomfort. Children do not feel the normal sensations that generally warn of impending injury such as drying of the eyes, pressure over pressure points, and

37. Riley-Day Syndrome rileyday syndrome. A Medical Arundel Hospital. A resource with informationon over 4000 medical topics including riley-day syndrome. http://www.marylandradiology.com/medical-terms/03550.htm

Riley-Day syndrome A Medical Encyclopedia Article provided by North Arundel Hospital A resource with information on over 4000 medical topics including: Riley-Day syndrome Previous Next

38. HONselect - Dysautonomia, Familial Type III Hereditary-Sensory and Autonomic Neuropathy Type III - Neuropathy, Hereditaryand Autonomic, Type III - riley-day syndrome - Dominant Hereditary http://www.hon.ch/HONselect/RareDiseases/C10.177.272.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Dysautonomia, Familial - HSAN Type III - Hereditary-Sensory and Autonomic Neuropathy Type III - Neuropathy, Hereditary and Autonomic, Type III - Riley-Day Syndrome - Dominant Hereditary Sensory Neuropathy, Type III - HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III Français: DYSAUTONOMIE FAMILIALE - DESEQUILIBRE NEUROVEGETATIF FAMILIAL - RILEY-DAY, SYNDROME Deutsch: Dysautonomie, familiäre - Heriditäre-sensorische-autonome Neuropathie Typ III - HSAN-Typ III - Neuropathie, heriditäre und autonome, Typ III - Riley-Day-Syndrom Español: DISAUTONOMIA FAMILIAR - NEUROPATIA HEREDITARIA-SENSORIAL Y AUTONOMA TIPO III - HSAN TIPO III - NEUROPATIA AUTONOMA Y HEREDITARIA-SENSORIAL TIPO III - SINDROME DE RILEY-DAY Português: DISAUTONOMIA FAMILIAR - NEUROPATIA HEREDITARIA SENSORIAL E AUTONOMA TIPO III - HSAN TIPO III - NEUROPATIA HEREDITARIA E AUTONOMA TIPO III - SINDROME DE RILEY-DAY - NEUROPATIA SENSORIAL E AUTONOMA HEREDITARIA TIPO III HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: No Web sites: English Yes Français No Deutsch No Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C10.177.272.html

39. List Of Rare Disease Or Syndrome Reye syndrome, Digestive System Diseases, Yes, Yes, Yes, rileyday syndrome, NervousSystem Diseases, Yes, Yes, Romano-Ward syndrome, Cardiovascular Diseases, Yes, Yes,Yes. http://www.hon.ch/HONselect/RareDiseaseRS.html

List of Rare disease or syndrome A B C D ... P - Q- R S T - U- V W - X- Y- Z Rare disease or syndrome MeSH category Definition Articles Web pages Images Rasmussen encephalitis Virus Diseases Yes Yes Yes Yes ... Raynaud's disease/phenomenon Cardiovascular Diseases Yes Yes Yes Refsum syndrome Nervous System Diseases Yes Yes Yes Yes ... Reiter syndrome Bacterial Infections and Mycoses Yes Yes Yes Rett syndrome Nervous System Diseases Yes Yes Yes Reye syndrome Digestive System Diseases Yes Yes Yes Riley-Day syndrome Nervous System Diseases Yes Yes Romano-Ward syndrome Cardiovascular Diseases Yes Yes Yes Romberg hemi-facial atrophy Stomatognathic Diseases Yes Yes Yes Rosai-Dorfman disease Hemic and Lymphatic Diseases Yes Yes Rothmund-Thomson syndrome Neonatal Diseases and Abnormalities Yes Yes Roussy-Levy syndrome Nervous System Diseases Yes Yes Rubinstein-Taybi syndrome Musculoskeletal Diseases Yes Yes Rare disease or syndrome MeSH category Definition Articles Web pages Images Saethre-Chotzen syndrome Musculoskeletal Diseases Yes Yes Yes Yes ... Sandhoff disease Nervous System Diseases Yes Yes Yes Sanfilippo syndrome Skin and Connective Tissue Diseases Yes Yes Yes Schamberg disease Skin and Connective Tissue Diseases Yes Yes Scheurermann ('s) Disease Musculoskeletal Diseases Yes Yes Yes Yes ... Schmidt syndrome Endocrine Diseases Yes Yes Seitelberger disease Nervous System Diseases Yes Yes Sheehan syndrome Nervous System Diseases Yes Yes Yes Yes ... Shwartzman phenomenon Cardiovascular Diseases Yes Yes Shy-Drager syndrome Nervous System Diseases Yes Yes Yes Sjogren Larsson syndrome Neonatal Diseases and Abnormalities

40. Familial Dysautonomia (Riley-Day Syndrome) Disease Familial dysautonomia (rileyday syndrome). OMIM number 223900. BodySystem Neurological neuromuscular. Type -. Inheritance pattern AR. http://archive.uwcm.ac.uk/uwcm/mg/fidd/pages/845.html

Disease : Familial dysautonomia (Riley-Day syndrome) OMIM number : Body System : Type : Inheritance pattern : AR Incidence/prevalence : I Population surveyed : Israel (Jews, Ashkenazi) Date of survey : Number of cases : Size of population surveyed : Frequency figure (1 in ...) : Frequency figure for females : Method (direct/indirect) : D Reference : Moses SWY, Rotem N, Jagoda N, Talmor N, Eichhorn F, Levin S. A clinical, genetic and biochemical study of familial dysautonomia in Israel. Israel J Med Sci 1967;3:358-371. Comments : Cases aged 7 months to 19 years.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 2     21-40 of 96    Back | 1  | 2  | 3  | 4  | 5  | Next 20