Nnjm2: Added some links.

2017-12-04T21:54:15Z

Added some links.

← Older revision		Revision as of 21:54, 4 December 2017
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	Any disruption of galactose metabolism is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in galactose 1-phosphate uridyl transferase activity. Infants afflicted cannot thrive, and symptoms include vomiting, ~~diarrhea~~ after consuming milk. Liver ~~enlargment~~ and jaundice are also common, which may also lead to cirrhosis. Cataracts can form, which may also be followed by lathargy and retarded mental development. Level of galactose in blood is significantly increased, and galactose may also be found in urine. The definitive diagnostic criterion is the absence of the enzyme transferase in red blood cells.		Any disruption of [[galactose metabolism\|galactose metabolism]] is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in [[galactose 1-phosphate uridyl transferase\|galactose 1-phosphate uridyl transferase]] activity. Infants afflicted cannot thrive, and symptoms include vomiting, diarrhoea after consuming milk. [[Liver\|Liver]] enlargement and [[jaundice\|jaundice]] are also common, which may also lead to [[cirrhosis\|cirrhosis]]. Cataracts can form, which may also be followed by lathargy and retarded mental development. Level of galactose in blood is significantly increased, and galactose may also be found in urine. The definitive diagnostic criterion is the absence of the enzyme transferase in red blood cells.

	The most common treatment is to remove galactose (as well as lactose) from the diet. Although this will prevent liver disease and cataract development, the majority of patients may still suffer from CNS malfunction, usually related to delayed development of language skills. Ovarian failure is also a possibility in female patients<sup><ref>Berg J, Tymoczko J and Stryer L. (2012) Biochemistry, 7th edition, New York: WH Freeman. pg468</ref></sup>.		The most common treatment is to remove [[galactose\|galactose]] (as well as [[lactose\|lactose]]) from the diet. Although this will prevent liver disease and cataract development, the majority of patients may still suffer from [[Central_nervous_system\|CNS]] malfunction, usually related to delayed development of language skills. Ovarian failure is also a possibility in female patients<sup><ref>Berg J, Tymoczko J and Stryer L. (2012) Biochemistry, 7th edition, New York: WH Freeman. pg468</ref></sup>.

	Appropriate treatment (i.e., antibiotic drugs) may be used to control infection. The emotional effects of the strict diet may require additional help and supportive measures throughout childhood. Genetic ~~counseling~~ is also highly recommended for persons with children who have galactosemia<ref>National Organization for Rare Disorders, Galactosemia. Date accessed: [3/12/2017]. Available from :https://rarediseases.org/rare-diseases/galactosemia/</ref>.		Appropriate treatment (i.e., [[Antibiotic\|antibiotic]] drugs) may be used to control infection. The emotional effects of the strict diet may require additional help and supportive measures throughout childhood. Genetic counselling is also highly recommended for persons with children who have galactosemia<ref>National Organization for Rare Disorders, Galactosemia. Date accessed: [3/12/2017]. Available from :https://rarediseases.org/rare-diseases/galactosemia/</ref>.

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170221843: Created page with "Any disruption of galactose metabolism is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in galactose 1-phosphat..."

2017-12-03T22:28:41Z

Created page with "Any disruption of galactose metabolism is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in galactose 1-phosphat..."

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Any disruption of galactose metabolism is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in galactose 1-phosphate uridyl transferase activity. Infants afflicted cannot thrive, and symptoms include vomiting, diarrhea after consuming milk. Liver enlargment and jaundice are also common, which may also lead to cirrhosis. Cataracts can form, which may also be followed by lathargy and retarded mental development. Level of galactose in blood is significantly increased, and galactose may also be found in urine. The definitive diagnostic criterion is the absence of the enzyme transferase in red blood cells.

The most common treatment is to remove galactose (as well as lactose) from the diet. Although this will prevent liver disease and cataract development, the majority of patients may still suffer from CNS malfunction, usually related to delayed development of language skills. Ovarian failure is also a possibility in female patients<sup><ref>Berg J, Tymoczko J and Stryer L. (2012) Biochemistry, 7th edition, New York: WH Freeman. pg468</ref></sup>.

Appropriate treatment (i.e., antibiotic drugs) may be used to control infection. The emotional effects of the strict diet may require additional help and supportive measures throughout childhood. Genetic counseling is also highly recommended for persons with children who have galactosemia<ref>National Organization for Rare Disorders, Galactosemia. Date accessed: [3/12/2017]. Available from :https://rarediseases.org/rare-diseases/galactosemia/</ref>.

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Galactosemia - Revision history

Nnjm2: Added some links.

170221843: Created page with "Any disruption of galactose metabolism is referred to as ''galactosemia''. Classic galactosemia is the most common type, and it is an inherited deficiency in galactose 1-phosphat..."