What does the medical abbreviation PKU mean?

Answer 1

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Answer 2

PKU stands for phenylketonuria.

Answer 3

iii

Answer 4

what's galactosemia is worst? type1 classic galt| very sever. gale epimerase deficiency| type4 gale| modrat/severe. galk deficiency (GALK)| type2 galactosemia. is a mild type of galactosemia. or duarte galactosemia is a mild variant of classic galactosemia| type 3 galc?

what's wors: galactosemia. pku. anaphylaxis. or: lactose intolerance?

Answer 5

galactosemia, which means “galactose in the blood,” refers to a group of inherited disorders that impair the body's ability to process and produce energy from a sugar called galactose. When people with galactosemia injest foods or liquids containing galactose, undigested sugars build up in the blood. classic galactosemia (type 1) - the most common and severe type, caused by mutations in the GALT gene, and characterized by a complete deficiency of an enzyme called galactose-1-phosphate uridyl transferase (GALT). type IV galactosemia is likely to result in a buildup of β-d-galactose. In type I and type III galactosemia, the buildup of galactose 1-phosphate has been proposed to be responsible for many of the manifestations of these diseases. duarte galactosemia is a specific type of galactosemia. galactosemias are a group of rare inherited conditions. galactosemia means “galactose in the blood.” people with duarte galactosemia digest a type of sugar called galactose more slowly. galactose is found in milk and all foods that contain milk. classic galactosemia (GALT) is an inherited condition in which the body is unable to properly digest galactose, a sugar found in all foods that contain milk. If a child with GALT eats galactose, undigested sugars build up in the blood rather than being used for energy. classic galactosemia, also known as type I, is the most common and most severe form of the condition. If infants with classic galactosemia are not treated promptly with a low-galactose diet, life-threatening complications appear between birth or atleast by within a few day's after birth.

type4: moderate/severe. type 3 affected infants develop cataracts but otherwise experience few long-term complications. the signs and symptoms of galactosemia type III vary from mild to severe and can include cataracts, delayed growth and development, intellectual disability, liver disease, and kidney problem's. mild/severe.

galactosemia type II (also called galactokinase deficiency) and type III (also called galactose epimerase deficiency) cause different patterns of signs and symptoms. galactosemia type II causes fewer medical problems than the classic type. galactosemia type II causes fewer medical problems than the classic type. affected infants develop cataracts but otherwise experience few long-term complications| mild/moderate. classic galactosemia is a rare, serious, life-threatening disorder. duarte galactosemia is more common and usually causes no symptom's, but. duarte galactosemia is an inherited condition associated with diminished ability to metabolize galactose due to a partial deficiency of the enzyme galactose-1-phosphate uridylyltransferase| mild

Answer 6

Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a building block of proteins (an amino acid) that is obtained through the diet.

Symptoms: Brain damage; Intellectual disability

Answer 7

what's wors: galactosemia. anaphylaxis. or: pku. or: lactose intolerance

Answer 8

for: galactosemia: severities. true or false: type1| severe type4| moderate/severe type3| mild/severe type2| mild/moderate durate| mild?

Answer 9

what's wors: galactosemia or: pku?

Answer 10

b