Extractions: 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.
Extractions: 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 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.
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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
Extractions: 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.
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
Extractions: 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.
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
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
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
Extractions: needs and parents with special needs children. 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.
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
Acidemia, Propionic propionic acidemia is a rare metabolic disorder characterized by deficiency of propionylCoA carboxylase, an enzyme involved in the breakdown (catabolism) of http://my.webmd.com/hw/health_guide_atoz/nord500.asp
Extractions: 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.
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
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
Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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.
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
Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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.
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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
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
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
Propionic Acidemia: A Neuropathology Case Report And Review Of Prior Cases e325e328. 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
