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         Propionic Acidemia:     more detail
  1. Propionic acidemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Linnea, MS Wahl, 2005
  2. Propionic Acidemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18

21. ,Acidemia Propionic,Propionic Acidemia,Type I (PCCA Deficiency),Type II (PCCB De
Type I (PCCA Deficiency),Acidemia Propionic,propionic acidemia,Type II (PCCB Deficiency),Hyperglycinemiawith Ketoacidosis and Lactic Acidosis Propionic Type
http://www.icomm.ca/geneinfo/acidprop.htm
Type I (PCCA Deficiency),Acidemia Propionic,Propionic Acidemia,Type II (PCCB Deficiency),Hyperglycinemia with Ketoacidosis and Lactic Acidosis Propionic Type,Ketotic Glycinemia,Propionyl CoA Carboxylase Deficiency
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
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DISORDERS GLOSSARY Acidemia, Propionic
also known as:
Hyperglycinemia with Ketoacidosis
and Lactic Acidosis, Propionic Type
Ketotic Glycinemia
PCC Deficiency
Propionyl CoA Carboxylase Deficiency Disorder Subdivisions Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency) (as defined at http://www.pafoundation.com/pages/869032/index.htm The Propionic Acidemia Foundation (PAF))
WHAT IS PROPIONIC ACIDEMIA? Propionic acidemia is a genetic disorder of branched-chain amino acid metabolism. Odd chain fatty acids and cholesterol are also not metabolized correctly by PA patients, but the bulk of the damage to the body comes from consuming a diet too high in protein. Individuals with PA build up propionic acid and other toxins in their bodies if they consume too much protein containing the amino acids methionine, threonine, isoleucine and valine.

22. Propionic Acidemia,Hyperglycinemia With Ketoacidosis And Lactic Acidosis Propion
propionic acidemia,Hyperglycinemia with Ketoacidosis and Lactic Acidosis PropionicType,Ketotic Glycinemia,PCC Deficiency,Propionyl CoA Carboxylase Deficiency
http://www.icomm.ca/geneinfo/propacid.htm
Propionic Acidemia,Hyperglycinemia with Ketoacidosis and Lactic Acidosis Propionic Type,Ketotic Glycinemia,PCC Deficiency,Propionyl CoA Carboxylase Deficiency,Propionic Acidemia Type I (PCCA Deficiency),Propionic Acidemia, Type II (PCCB Deficiency For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
HOME
DISORDERS GLOSSARY Propionic Acidemia
also known as:
Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
Ketotic Glycinemia
PCC Deficiency
Propionyl CoA Carboxylase Deficiency
Disorder Subdivisions
Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency)
Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result.

23. Genetic Disorders, Propionic Acidemia
Submit Your Site to the propionic acidemia category. Sponsored PropionicAcidemia Sites. Submit Your Site to the propionic acidemia category.
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24. Genetic Disorders, Propionic Acidemia
Category Home Health Conditions and Diseases Genetic Disorders propionic acidemia. * Site Title · The name of the site.
http://www.iseekhealth.com/directory/index.php?method=show_link_exchange&directo

25. Propionic Acidemia
Click Here! propionic acidemia. propionic acidemia is inherited as an autosomalrecessive trait. Remedy. Characteristics Symptoms. Patient Worse by.
http://www.stormloader.com/users/saibabaservs/Propionic Acidemia.htm
Propionic Acidemia Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait Remedy Characteristics Symptoms Patient Worse by Patient Better by Nux Vomica Rather thin, spare, quick, active, nervous, and irritable Does a good deal of mental work; has mental strains and leads a sedentary life, found in prolonged office work, overstudy, and close application to business, with its cares and anxieties.

26. Diseases & Conditions
Acidemia, Propionic New propionic acidemia is a rare metabolic disorder characterizedby deficiency of propionyl CoA carboxylase, an enzyme involved in the
http://www.stormloader.com/users/saibabaservs/Diseases & Conditions.htm
Click on the health condition applicable for you to find the possibly suitable remedies with their characteristic symptoms and the modalities of patient. The modalities of patient are the conditions which makes the patient generally worse or better. The suitable remedy is the one which matches your symptoms and modalities most. As explained earlier, you need not have all the symptoms and modalities listed under the remedy. Once having identified, please ensure that you take only one dose of the 30c potency of the selected remedy because repetition without proper evaluation could either cause severe aggravation or waste the remedy. Please remember that this is not a substitute for proper consultation with a Homeopath. In case of any doubt, please consult a homeopath locally or E Mail us. ACTH Deficiency ACTH Deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure (hypotension). The pituitary hormone called "adrenocorticotropic hormone" (ACTH) is decreased or absent, and other cortisol and other steroid hormone levels in the blood are abnormally low. AIDS (Acquired Immune Deficiency Syndrome) AIDS is an infectious disorder that suppresses the normal function of the immune system. It is caused by the human immunodeficiency virus (HIV), which destroys the body's ability to fight infections. Specific cells of the immune system that are responsible for the proper response to infections (T cells) are destroyed by this virus. Characteristically a person infected with HIV initially experiences no symptoms for a variable period of time. This may be followed by the development of persistent generalized swelling of the lymph nodes (AIDS-related lymphadenopathy). Eventually most patients infected with HIV experience a syndrome of symptoms that includes excessive fatigue, weight loss, and/or skin rashes.

27. Conditions And Diseases - Propionic Acidemia Top Links
propionic acidemia Web Site Links. Pediatric Database Offers investigationsand management. eMedicine - An in depth look at propionic acidemia.
http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
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Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health
Propionic Acidemia Web Site Links Pediatric Database Offers a definition of propionic acidemia as well as the epidemiology, pathogenesis, clinical features, investigations and management.
eMedicine
An in depth look at Propionic acidemia.
Cadence's Story
The story of one little girl's life with the genetic disease Propionic Acidemia.
NORD - Acidemia, Propionic
Includes the synonyms, a general discussion and further resources.
Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research.
AHRQ: Clinical Information
Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse.
The UK Health Technology Assessment Programme
Site contains details of program's many projects and publications; an NHS national research and development initiative.
U.S. Preventive Services Task Force (USPSTF)

28. Inborn Errors Of Metabolism: Organic Acidemia Association
propionic acidemia Q A. by Dr. Alan Greene. Question Some friends of minerecently had a baby who was diagnosed with propionic acidemia.
http://www.oaanews.org/article.asp?article=113

29. Genetic Disorders: Propionic Acidemia
Genetic Disorders propionic acidemia. Breastfeeding a child with propionicacidemia is discussed in this question and answer format. eMedicine.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Pr
Genetic Disorders: Propionic Acidemia
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Standard Listings
Dr. Greene: Breastfeeding with a Metabolic Disorder and Propionic Acide...
Breastfeeding a child with propionic acidemia is discussed in this question and answer format.
eMedicine
An in depth look at Propionic acidemia.
NORD: Acidemia, Propionic
Includes the synonyms, a general discussion and further resources.
Pediatric Database
Offers a definition of propionic acidemia as well as the epidemiology, pathogenesis, clinical features, investigations and management.
Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor PureDirectory.com uses a modified version of the Open Directory.

30. EPEC - Educating Parents Of Extra-special Children - Propionic Acidemia
propionic acidemia. propionic acidemia is findings. propionic acidemiais inherited as an autosomal recessive trait. Clinical symptoms
http://www.epeconline.com/PropionicAcidemia.html
Educating Parents of Extra-special Children (EPEC)
A resource of information for adults with special
needs and parents with special needs children.
Propionic Acidemia
Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait. Clinical symptoms of propionic acidemia include metabolic acidosis, hyperammonemia, vomiting, failure-to-thrive, lethargy, respiratory distress, and coma. Untreated, a child may suffer from irreversible brain damage and death. Symptoms may be prevented and the disorder may be managed by diet.

31. A To Z Encyclopedia Topic: Propionic Acidemia
Metabolism Program. Unfortunately, at this time, we are not able toprovide information about this condition or procedure. However
http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Propionic Acidemia

32. Acidemia, Propionic
propionic acidemia is a rare metabolic disorder characterized by deficiency of propionylCoA carboxylase, an enzyme involved in the breakdown (catabolism) of
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You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Acidemia, Propionic Important It is possible that the main title of the report Acidemia, Propionic is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • PCC Deficiency Propionyl CoA Carboxylase Deficiency Ketotic Glycinemia Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
Disorder Subdivisions
  • Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency)
General Discussion Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait.

33. Propionic Acidemia
HOME. propionic acidemia. Proprionic Acidemia; Coincidence of PKUand propionic acidemia in an Amish girl; propionic acidemia; Three
http://www.bdid.com/propacid.htm

HOME
Propionic Acidemia

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34. Acidemia, Propionic
propionic acidemia is a rare metabolic disorder characterized by deficiency of propionylCoA carboxylase, an enzyme involved in the breakdown (catabolism) of
http://www.bchealthguide.org/kbase/nord/nord500.htm
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National Organization for Rare Disorders, Inc.
Acidemia, Propionic
Important
It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • PCC Deficiency Propionyl CoA Carboxylase Deficiency Ketotic Glycinemia Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
Disorder Subdivisions
  • Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency)
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Ketotic Hyperglycinemia Methylmalonic Acidemias
General Discussion
Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait.

35. Valinemia
propionic acidemia; . Related disorders include maple syrup urine disease, propionicacidemia, methylmalonic acidemia, and multiple carboxylase deficiency.
http://www.bchealthguide.org/kbase/nord/nord627.htm
document.write(''); var hwPrint=1; var hwDocHWID="nord627"; var hwDocTitle="Valinemia"; var hwRank="1"; var hwSectionHWID="nord627"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD";
National Organization for Rare Disorders, Inc.
Valinemia
Important
It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • Hypervalinemia Valine Transaminase Deficiency
Disorder Subdivisions
  • None
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Maple Syrup Urine Disease Methylmalonic Acidemias Multiple Carboxylase Deficiency Propionic Acidemia
General Discussion
Valinemia is a very rare metabolic disorder. It is characterized by elevated levels of the amino acid valine in the blood and urine caused by a deficiency of the enzyme valine transaminase. This enzyme is needed in the breakdown (metabolism) of valine. Infants with valinemia usually have a lack of appetite, vomit frequently, and fail to thrive. Low muscle tone (hypotonia) and hyperactivity also occur.
The breakdown of valine involves at least seven stages and a deficiency of the appropriate enzyme at any of these stages leads to a disorder of varying severity and rarity.

36. :: Ez2Find :: Propionic Acidemia
Guide propionic acidemia, Global Metasearch Any Language Guides, propionic acidemia.ez2Find Home Directory Health
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Web Sites

37. Conditions And Diseases: Genetic Disorders: Propionic Acidemia
Health and Home. propionic acidemia. rdbdetail_abstract.html?disname=Acidemia%2C%20Propionic.propionic acidemia. Last Update Mon May 10 2004.
http://www.health-home.net/Conditions_and_Diseases/Genetic_Disorders/Propionic_A
Health and Home
Propionic Acidemia
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Looking for something in particular? the entire directory only this category Home Conditions and Diseases Genetic Disorders : Propionic Acidemia LINKS:
  • Pediatric Database
    Offers a definition of propionic acidemia as well as the epidemiology, pathogenesis, clinical features, investigations and management.
    http://www.icondata.com/health/pedbase/files/PROPIONI.HTM
  • Dr. Greene: Breastfeeding with a Metabolic Disorder and Propionic Acidemia
    Breastfeeding a child with propionic acidemia is discussed in this question and answer format.
    http://www.drgreene.com/21_692.html
  • eMedicine
    An in depth look at Propionic acidemia.
    http://www.emedicine.com/NEURO/topic577.htm
  • NORD: Acidemia, Propionic Includes the synonyms, a general discussion and further resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Acidemia%2C%20Propionic
Propionic Acidemia
Last Update: Mon May 10 2004

38. Propionic Acidemia Foundation
Return to Search Page propionic acidemia Foundation. Email pafoundation@attbi.com.Conditions propionic acidemia. Year Established 2002
http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Prop

39. Propionic Acidemia
Directory, Home Health Conditions and Diseases Genetic Disorders PropionicAcidemia (4) See Also eMedicine An in depth look at propionic acidemia.
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/Pr
Directory Home Health Conditions and Diseases Genetic Disorders : Propionic Acidemia (4)
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40. Propionic Acidemia: A Neuropathology Case Report And Review Of Prior Cases
e325–e328. propionic acidemia A Neuropathology Case Report and Review of PriorCases. Vacuolization in propionic acidemia may result from a similar process.
http://arpa.allenpress.com/arpaonline/?request=get-document&doi=10.1043/1543-216

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