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Like many genetic disorders galactosemia is a disruption of a metabolic pathway due to a malfunctioning?
Wiki User
∙ 9y ago
Many genetic orders such as galactosemia is a disruption in a metabolic pathway. Galactosemia is a disruption in the process of breaking down galactose.
Wiki User
∙ 9y ago
Anonymous
Anonymous
What is the difference between lactose intolerance and galactosemia? No, galactosemia should not be confused with lactose intolerance. People with galactosemia usually have no problems digesting lactose or absorbing galactose. ... People who are lactose intolerant must avoid large amounts of lactose in foods but can usually still digest and metabolize galactose. Nov 13, 2014 soo not true, swich arround!
galactosemia is wors then lactose intolerance! galt can't digest milk, dairy or lactose or anything: dairy! People with galactosemia usually have no problems digesting lactose or absorbing galactose? uumm,.... lie! People with galactosemia i think do have problem's problems digesting lactose or absorbing galactose! People who are lactose intolerant must avoid large amounts of lactose in foods but can usually still digest and metabolize galactose. People who are lactose intolerant must avoid large amounts of lactose in foods but can usually still digest and metabolize galactose? lie! li can have, maby just a littlebit of digest milk, dairy or lactose or anything: dairy! galactosemia is way wors then li is! look up galactosemia! galactosemia can't digest! li can mabyjust a littlebit?
Anonymous
Anonymous
Anonymous
Can you grow out of galactosemia? Galactosemia is a lifelong condition that children will not outgrow. However, galactosemia can be easily managed by following a galactose-free diet. ... The majority of fruits, vegetables, grains, breads, fats, and sugars are safe to eat as long as they contain little or no galactose. Oct 10, 2019 supposedlly, no. u can't outgrow it, it's a lifetime thing u have 2 deal with, i think?
Anonymous
There are three main types of galactosemia:
Classic (type I) sever type
Galactokinase deficiency (type II) mild/modrat?
Galactose epimerase deficiency (type III) mild?
Anonymous
Anonymous
how sever is each galt disorder? sever type1 classic, durate type2 virant galactosemia, type3 defencisce galactosemia, or type4 defensecie epimerase?
Anonymous
Anonymous
Anonymous
classic galactosemia
duarte galactosemia
galactokinase deficiency
galactose epimerase deficiency
Anonymous
Anonymous
how r u born with: galactosemia?
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The body's rate of kilocalorie consumption needed to fuel all ongoing activities is called the?
basal metabolic rate. Its not basal metabolic rate because The basal metabolic rate (BMR) is the energy the body needs to perform only its most essential activities such as breathing and maintaining resting levels of organ function. Total Metabolic Rate because The total metabolic rate (TMR) is the rate of kilocalorie consumption needed to fuel all ongoing activities (involuntary and voluntary).
What process does thyroxin control?
Thyroxine is a hormone, or chemical messenger, that is secreted by the thyroid gland to help regulate metabolic processes and influence physical development of the body.
What is the body's rate of kilocalorie consumption needed to fuel all ongoing activities is called?
Total Metabolic Rate
What category does bronchitis go under metabolic infectious genetic or acquired?
Acquired. As it is caused by environmental and lifestyle facotrs such as smoking. In particular it is an example of chronic obstructive pulmonary disease (COPD).
What kind of molecule is G3P?
Glyceraldehyde 3-phosphate, also known as triose phosphate or G3P, is an organic compound. It occurs as an intermediate in several central metabolic pathways of all organisms.
Is galactosemia sex-linked?
No, it is a genetic metabolic disorder.
Galactosemia is the name of a metabolic disorder In this disorder an enzyme is missing that is needed to?
...that is needed to break down galactose.
What is a metabolism disorder?
Metabolic disorders refers to diseases or disorders of the internal body chemistry that causes the body's metabolism. The term metabolic disorders usually does not include hormonal disorders or endocrine disorders which refer to the interactions between body glands and hormones.
How do you treat a metabolic disorder?
The main treatment for metabolic disorders is changing your lifestyle.There are many treatments but this one seems to be the most safe and effective for people with these disorders.
Why are newborns tested for metabolic disorders?
Metabolic disorders are rare disorders routinely tested for in a newborn baby. It is always better to know the presence of these diseases before hand and not after it the child starts showing symptoms for it. To avoid unnecessary suffering to the baby this test is done before for as many as 100 disorders. The disease manifests in many ways , it can also lead to mental retardation in your baby. Metabolic disorders can be screened as early as after 48hrs of birth of that baby. Metabolic disorders lead to irreversible mental damage. Screening for disorders will help in early intervention of therapy and will give a better life to that baby. Nowadays there are screening done from urine sample and for a large range of metabolic disorders.
The endocrine gland that is probably malfunctioning if a person has a high metabolic rate is the parathyroid?
the thyroid gland
What is Mucopolysaccharidosis?
Mucopolysaccharidosis is a group of autosomal recessive metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called glycosaminoglycans - long chains of sugar carbohydrates in each of our cells that help build bone, cartilage, tendons ...
What structure in the brain regulates body temperature eating and drinking?
disruption of metabolic processes in the metabolic system
Why is urine used as a sample over blood when testing for genetic metabolic disorders?
Urine is the preferred sample when testing for acidemia in metabolic disorders. The general researchers says that the metabolites appear in urine first and take longer to be detected in blood, making the urine sample as the preferred sample for screening and diagnosis of rare 100 metabolic disorders. Metabolites appear first in the urine and later in the blood, making pre-symptomatic detection of metabolic disorders possible from urine sample. Its a Non-invasive process for screening of metabolic disorders, hence its Baby-friendly. Therapy and Management of these disorders at its earliest will help to curb any damage to the baby.
What is the comprehensive panel metabolic screening for newborn babies?
Comprehensive panel metabolic screening is done on newborn babies to test for genetic disorders from birth. The panel comprises of many rare metabolic disorders which individually might occure very rare but when seen collectively the occurrence increase many fold. There are more than 100 metabolic disorders which can be detected in a newborn urine sample.
What has the author Leonard Sinclair written?
Leonard Sinclair has written: 'Metabolic disease in childhood' -- subject(s): Metabolic Diseases, Metabolic disorders in children, In infancy & childhood
What are some of the diseases that a neuropathologist deals with?
This range of disease includes degenerative diseases, infections, metabolic disorders, immunologic disorders, disorders of blood vessels, and physical injury.
