61. Your Health - Galactosemia with each other. galactosemia. by Michelle Badash, MS. Definition. Classic galactosemia is an inherited disease. Due to a http://www.aurorahealthcare.org/yourhealth/healthgate/getcontent.asp?URLhealthga

62. Fast Facts Galactosemia Fast Facts. GENETIC LIVER DISEASES galactosemia What is it? This diet must be continued for years, and possibly for life. How prevalent is galactosemia? http://www.aasld.org/netFORUMAASLD/eweb/DynamicPage.aspx?webcode=FastFacts_Gas

63. Liver Disease In Saudi Arabia - Liver Diseases - Galactosemia Wilson Disease. Alpha1-antitrypsin Deficiency. galactosemia. Liver Diseases - galactosemia. Under Construction. Signs and Symptoms Diagnosis Treatment http://www.liverme.org/liver_diseases/galactosemia.htm

64. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor News about galactosemia More news about galactosemia . Books about galactosemia More books about galactosemia . Links about galactosemia http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica

Match: sort by: relevance date Free Services Subscribe by email RSS newsfeeds PDA-friendly format loc="/images/" A A A Find Jobs In: Healthcare Engineering Accounting College Contract / Freelance Customer Service Diversity Engineering Executive Healthcare Hospitality Human Resources Information Tech International Manufacturing Nonprofit Retail All Jobs by Job Type All Jobs by Industry Relocating? Visit: Moving Resources Moving Companies Mortgage Information Mortgage Calculator Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Metabolic Galactosemia (3 links) See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders News about Galactosemia [ More news about Galactosemia Books about Galactosemia [ More books about Galactosemia Links about Galactosemia Parents of Galactosemic Children, Inc. - Information about galctosemia and a resource for families living with galactosemia. National Library of Medicine: GALC - The alternate names, a summary and list of major features of galactocerebrosidase deficiency. NORD - Galactosemia - Offers the synonyms, a general discussion and further resources.

65. Galactosemia Biotinidase Deficiency, Congenital Adrenal Hyperplasia, Fatty Acid Oxidation Disorders, galactosemia, Hemoglobinopathies, Hypothyroidism, Organic Acid Disorders, http://www.uhl.uiowa.edu/services/mychildshealth/newborn/disorders/galactosemia.

Testing and Services News Room Contact Us About UHL ... Site Map Search Quick Links Well Water Today's Air Quality Disease / Infection / Illness Info Environmental Info Kits / Quotes / Forms Results Interpretation Laboratory Certification Terrorism and Emergency Response Amino Acid Disorders Biotinidase Deficiency Congenital Adrenal Hyperplasia Fatty Acid Oxidation Disorders ... Disorders Galactosemia Babies born without a certain enzyme cannot break down the milk sugar, called galactose. As galactose builds up in the blood stream, life-threatening complications to the brain and liver can occur as early as the first week of life. With early diagnosis and placing the baby on a special milk-free diet, these problems can be prevented. This inherited disorder occurs in about 1 in every 70,000 births. Web Master Site Map

66. Galactosemia Cystinuria. galactosemia. Gaucher Disease. Glycogen Storage Disease. Urea Cycle Defects. galactosemia. This area will soon contain updated information. http://www.vanhosp.bc.ca/html/wellness_amdc_findout_galactosemia.html

Home Adult Metabolic Diseases Find Out About a Specific Disease Adreno-leukodystrophy ... Cystinuria Galactosemia Gaucher Disease Glycogen Storage Disease Homocystinuria Maple Syrup Urine Disease ... Urea Cycle Defects Galactosemia This area will soon contain updated information. Please see the resources section for other sites of interest. About VHHSC Reaching Out Patient Info Health Professionals ... Employment Info

67. Galactosemia Terms of Use. galactosemia. Definition galactosemia. galactosemia. Noun. All rights reserved. Specialty Definitions galactosemia. Domain, Definitions. Health. http://www.websters-online-dictionary.org/definition/english/ga/galactosemia.htm

Philip M. Parker, INSEAD. Galactosemia Definition: Galactosemia Galactosemia Noun . A genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth. Source: WordNet 1.7.1 Specialty Definitions: Galactosemia Domain Definitions Health Buildup of galactose in the blood. Caused by lack of one of the enzymes needed to break down galactose into glucose. ( references Source: compiled by the editor from various references ; see credits. Top Crosswords: Galactosemia Specialty definitions using "galactosemia" Galactitol Galactokinase UDPglucose-Hexose-1-Phosphate Uridylyltransferase references ... Top Non-Fiction Usage: Galactosemia Subject Topic Quote Health Galactosemia , a rare genetic disorder, hampers the body's ability to process the sugar galactose. ( references Alpha-1 antitrypsin deficiency, hemochromatosis, Wilson's disease, galactosemia , and glycogen storage diseases are among the inherited diseases that interfere with the way the liver produces, processes, and stores enzymes, proteins, metals, and other substances the body needs to function properly. ( references Source: compiled by the editor from ICON Group International, Inc.

68. Galactosemia Management galactosemia Dietary Management Once galactosemia is suspected, the infant needs to be switched immediately to the soy formula ProSobee ® . http://www.meadjohnson.com/metabolics/galactosemiamanage.html

Galactosemia: Dietary Management Sandra Van Calcar, M.S., R.D. Biochemical Genetics Clinic, University of Wisconsin-Madison Madison, WI Once galactosemia is suspected, the infant needs to be switched immediately to the soy formula ProSobee . This formula contains only minute amounts of galactose compared with formulas made with cow’s milk. Affected infants can be fed ProSobee ad libitum at the standard dilution. Once solids are started at 4 to 6 months of age, parents must begin reading food labels to identify appropriate foods to give their young child. Baby food lists identifying acceptable foods are available (see Resource 1). A list of common foods and food ingredients that must be eliminated is provided in Table 1. Reading food labels is an essential component of managing galactosemia. Any food containing an ingredient with lactose or galactose must be eliminated from the diet. As the young child transitions to table foods, parents must continue to read food labels to identify any ingredients which are unacceptable in the diet for galactosemia. As the child matures, he or she can be involved in reading food labels as well and should become increasingly responsible for this task.

69. CCHS Clinical Digital Library galactosemia Clinical Resources. Miscellaneous galactosemia Clinical Resources Health Reviews for Primary Care Providers on the Internet Homepage http://cchs-dl.slis.ua.edu/clinical/metabolism/inborn/carbohydrate/galactosemia.

Clinical Resources by Topic: Metabolic Disorders Galactosemia Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Genetic Testing Clinical Resources General Genetic Disorders Clinical Resources General Metabolic Disorders Clinical Resources Galactosemia Patient/Family Resources Harrison's Principles of Internal Medicine 15th Ed.-2001: Table of contents Health Sciences Library subscription INFO Chapter 350: Glycogen Storage Diseases and Other Inherited Disorders of Carbohydrate Metabolism: Table of contents Other Muscle Glycogenoses with Muscle-Energy Impairment: Access document Introduction: Access document Disorders of Galactose Metabolism: Access document Galactose 1-phosphate Uridyl Transferase Deficiency Galactosemia: Access document Introduction: Access document Genetics: Access document Clinical and Laboratory Findings: Access document Treatment: Access document Galactokinase Deficiency: Access document Uridine Diphosphate Galactose 4-epimerase (UDP GAL 4-Epimerase) Deficiency: Access document Brenner and Rector's The Kidney 7th Ed.-2004 (MD Consult):

70. CCHS Clinical Digital Library galactosemia Patient/Family Resources. Galactose1-phosphate Uridyl Transferase English Spanish. Miscellaneous galactosemia Patient/Family Resources http://cchs-dl.slis.ua.edu/patientinfo/metabolism/inborn/carbohydrate/galactosem

Patient/Family Resources by Topic: Metabolic Disorders Galactosemia Patient/Family Resources Pediatrics Spanish Miscellaneous See also: Genetic Testing Patient/Family Resources General Genetic Disorders Patient/Family Resources General Metabolic Disorders Resources Galactosemia Clinical Resources Parents of Galactosemic Children Homepage What is Galactosemia?: Access document Frequently Asked Questions: Access document Info for the Newly Diagnosed: Access document MEDLINE plus Medical Encyclopedia: Table of contents Galactosemia: English Spanish Galactose-1-phosphate Uridyl Transferase: English Spanish Pediatrics Merck Manual - Second Home Edition Table of contents Section 23. Children's Health Issues: Table of contents Chapter 282. Hereditary Disorders of Metabolism: Table of contents Introduction: Access document Carbohydrate Metabolism Disorders: Access document Introduction: Access document Glycogen Storage Diseases: Access document Galactosemia: Access document Hereditary Fructose Intolerance: Access document Spanish MEDLINE plus Medical Encyclopedia: Table of contents Galactosemia: English Spanish Galactose-1-phosphate Uridyl Transferase: English Spanish Miscellaneous Galactosemia Patient/Family Resources The Family Village Library - Specific Diagnoses Card Catalog Table of contents Galactosemia: Access document Healthfinder (US DHHS): Homepage Galactosemia: List of documents National Library of Medicine MEDLINE plus Health Topics: Index Genetic Testing/Counseling: List of documents Genetic Disorders: List of documents YAHOO - Health:Diseases and Conditions:Metabolic Diseases Additional Metabolic Diseases resources (

71. Information Center - Galactosemia (Condition Description) ForMyDiet is designed to make living with and managing a galactosemia diet a whole lot easier. Helping galactosemia, Go Back. Author http://www.formydiet.com/Information/Doc.aspx?a=67

72. Utah Newborn Screening stick. Topics include PKU, blood spot, galactosemia, sickle cell, hemoglobinopathies and congenital hypothyroidism. galactosemia. http://www.health.utah.gov/newbornscreening/Galactosemia.htm

Galactosemia Fact Sheets Dietary Management Article: Galactosemia What causes the condition? The body cannot break down a certain sugar (galactose) found mostly in dariy products How often does it occur? One in 50,000 newborns What happens if it's not treated? Children become very sick (and may die). Mental retardation, cataracts and liver damage are possible. How is it treated? A special diet health.utah.gov Home Utah.gov Accessibility Policy

73. Galactosemia - Genetics Home Reference Genetic disorder catalog. galactosemia. What is galactosemia? galactosemia is a disorder of sugar metabolism. How common is galactosemia? http://ghr.nlm.nih.gov/condition=galactosemia

A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Galactosemia Related Gene(s) Quick links to this topic NIH Publications National Institutes of Health MedlinePlus Health Information Educational resources Information pages Patient support For patients and families Gene Reviews Clinical summary Gene Tests DNA test labs PubMed Recent literature OMIM Genetic disorder catalog Galactosemia What is galactosemia? Galactosemia is a disorder of sugar metabolism. This condition results when the body is not able to metabolize (break down) the sugar galactose, which is part of the sugar lactose, found in many foods but primarily in milk and other dairy products. Liver dysfunction, cataracts (clouding of the lens of the eye), speech problems, and mental impairment are characteristic of this condition. There are two main types of galactosemia, classic and Duarte variant. Individuals with the classic type of galactosemia lack the enzyme activity necessary to metabolize galactose. Individuals with the Duarte variant have approximately 5 to 20 percent of the enzyme activity necessary to metabolize this sugar and often do not have signs or symptoms of galactosemia. How common is galactosemia?

74. :: Búsqueda HispaVista : Galactosemia :: Translate this page RESULTADOS DE galactosemia. Se han encontrado 0 entradas en HispaVista. No se han encontrado coincidencias. Para hacer búsquedas http://buscador.hispavista.es/galactosemia/

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75. Neurological Disorders, Brain Diseases, Metabolic, Galactosemia More galactosemia Categories » Submit Your Site to the galactosemia category. Sponsored galactosemia Sites. Submit Your Site to the galactosemia category. http://www.iseekhealth.com/galactosemia-1954.php

Home About Us Contact Submit Your Site Search : Home Health Conditions and Diseases Neurological Disorders ... Galactosemia More Galactosemia Categories: Submit Your Site to the Galactosemia category Sponsored Galactosemia Sites Brain Disease. Is It Alzheimer's? Alzheimer's is a disease of the brain. It makes it hard for people to remember, think, and use language. It can also make it difficult to do daily tasks like using the phone and cooking. But early treatment may help. Learn how to spot early symptoms. Fully searchable traditional medicine and alternative medicine books, videos and products for doctors, students and the public. An affiliate of Amazon.com. PCBs May Cause Brain Damage and Memory Problems Because PCBs damage the thyroid gland, scientists believe PCBs may damage the brain and cause memory problems, along with altered thyroid hormone levels. National Library of Medicine: GALC - The alternate names, a summary and list of major features of galactocerebrosidase deficiency. NORD - Galactosemia - Offers the synonyms, a general discussion and further resources.

76. Disease - Galactosemia - Hartford, Connecticut , Saint Francis Care Disease galactosemia - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart disease http://www.saintfranciscare.com/12125.cfm

@import url(main.css); About Us Health Information Adam Article Manager CareMail Signup ... Ways To Help Adam Article Manager Back Back to main Health Information page Disease - Galactosemia Galactosemia Definition: Galactosemia is the inability of the body to use ( metabolize ) the simple sugar galactose (causing the accumulation of galactose 1-phosphate), which then reaches high levels in the body, causing damage to the liver, central nervous system, and various other body systems. Alternative Names: Galactose-1-phosphate uridyl transferase deficiency; Galactokinase deficiency; Galactose-6-phosphate epimerase deficiency Causes And Risk: Galactosemia is an inherited disorder (transmitted as an autosomal recessive trait). It occurs at a rate of approximately 1 out of 60,000 births. There are 3 forms of the disease galactose-1 phosphate uridyl transferase deficiency (classic galactosemia) and deficiency of galactose kinase or galactose-6-phosphate epimerase. Of these, the galactose-1-phosphate transferase deficiency is the most severe (and more common). People with galactosemia are unable to fully metabolize the simple sugar galactose. Galactose makes up half of the sugar, called lactose, that is found in milk. Lactose is called a disaccharide (di meaning 2 and saccharide meaning sugar) since lactose is made up of two sugars, galactose and glucose, bound together.

77. POF Support Group: Galactosemia And Turners Syndrome galactosemia AND TURNERS SYNDROME. Parents of Galactosemic Children, Inc. 2871 Stage Coach Drive Valley Springs, California 95252 http//www.galactosemia.org. http://www.pofsupport.org/information/resources/linkgts.htm

About the POFSG Contact Us Our Mission Our History ... Home GALACTOSEMIA AND TURNERS SYNDROME Parents of Galactosemic Children, Inc. 2871 Stage Coach Drive Valley Springs, California 95252 http://www.galactosemia.org Turner's Syndrome Society of the United States 1313 SE Fifth Street, Suite 327 Minneapolis, MN 55414 http://www.turner-syndrome-us.org Infertility Adoption Donor Egg / IVF ... Web Site Rules Would you like to submit a link for us to include in this resource list? email resources@pofsupport.org POF Support Group Website Rules Website Hosting - Hot Salsa Interactive

78. Galactosemia. The Columbia Encyclopedia, Sixth Edition. 2001 The Columbia Encyclopedia, Sixth Edition. 2001. galactosemia. (g l k´´t s ´m ) (KEY) , inherited metabolic disorder caused by http://www.bartleby.com/65/ga/galactsem.html

Select Search All Bartleby.com All Reference Columbia Encyclopedia World History Encyclopedia Cultural Literacy World Factbook Columbia Gazetteer American Heritage Coll. Dictionary Roget's Thesauri Roget's II: Thesaurus Roget's Int'l Thesaurus Quotations Bartlett's Quotations Columbia Quotations Simpson's Quotations Respectfully Quoted English Usage Modern Usage American English Fowler's King's English Strunk's Style Mencken's Language Cambridge History The King James Bible Oxford Shakespeare Gray's Anatomy Farmer's Cookbook Post's Etiquette Bulfinch's Mythology Frazer's Golden Bough All Verse Anthologies Dickinson, E. Eliot, T.S. Frost, R. Hopkins, G.M. Keats, J. Lawrence, D.H. Masters, E.L. Sandburg, C. Sassoon, S. Whitman, W. Wordsworth, W. Yeats, W.B. All Nonfiction Harvard Classics American Essays Einstein's Relativity Grant, U.S. Roosevelt, T. Wells's History Presidential Inaugurals All Fiction Shelf of Fiction Ghost Stories Short Stories Shaw, G.B. Stein, G. Stevenson, R.L. Wells, H.G. Reference Columbia Encyclopedia PREVIOUS NEXT ... BIBLIOGRAPHIC RECORD The Columbia Encyclopedia, Sixth Edition. galactosemia (g l s KEY ) , inherited metabolic disorder caused by an enzyme deficiency and transmitted as a recessive trait; it results in the accumulation of the sugar galactose in the body. The disorder is manifested soon after birth by feeding problems and diarrhea. Galactose is accumulated principally in the liver of the newborn infant, where it may induce cirrhosis, and in the lens of the eye, where cataracts may develop. Low glucose levels cause sufficient hypoglycemia to affect the central nervous system with resulting mental retardation. These ill effects can be prevented by removing milk and all other foods containing galactose and lactose from the diet.

79. Galactosemia. The American Heritage® Dictionary Of The English Language: Fourth galactosemia. The American Heritage® Dictionary of the English Language Fourth Edition. 2000. 2000. galactosemia. SYLLABICATION ga·lac·to·se·mi·a. http://www.bartleby.com/61/20/G0012000.html

Select Search All Bartleby.com All Reference Columbia Encyclopedia World History Encyclopedia Cultural Literacy World Factbook Columbia Gazetteer American Heritage Coll. Dictionary Roget's Thesauri Roget's II: Thesaurus Roget's Int'l Thesaurus Quotations Bartlett's Quotations Columbia Quotations Simpson's Quotations Respectfully Quoted English Usage Modern Usage American English Fowler's King's English Strunk's Style Mencken's Language Cambridge History The King James Bible Oxford Shakespeare Gray's Anatomy Farmer's Cookbook Post's Etiquette Bulfinch's Mythology Frazer's Golden Bough All Verse Anthologies Dickinson, E. Eliot, T.S. Frost, R. Hopkins, G.M. Keats, J. Lawrence, D.H. Masters, E.L. Sandburg, C. Sassoon, S. Whitman, W. Wordsworth, W. Yeats, W.B. All Nonfiction Harvard Classics American Essays Einstein's Relativity Grant, U.S. Roosevelt, T. Wells's History Presidential Inaugurals All Fiction Shelf of Fiction Ghost Stories Short Stories Shaw, G.B. Stein, G. Stevenson, R.L. Wells, H.G. Reference American Heritage Dictionary galactose ... BIBLIOGRAPHIC RECORD The American Heritage Dictionary of the English Language: Fourth Edition.

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

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