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2011-07-29 07:31:32
2011-07-29 07:31:32

In all disorders it might not be possible due to late diagnosis, but i know one case wherein my friends baby had fatty acid oxidation disorder where body cannot convert fat into glucose for energy, in such cases babies often expire unexpectedly , bt luckily for my friend he had already done newborn screening where the doctor came to know abt the disorder quite early and the treatment was started immediately which was feeding the child after every 2-3 hours and now their child is quite healthy.


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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.

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.

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.

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.

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.

Leonard Sinclair has written: 'Metabolic disease in childhood' -- subject(s): Metabolic Diseases, Metabolic disorders in children, In infancy & childhood

people with metabolic dis orders consult endocrinologist, (metabolic Harmone malfunction)

This range of disease includes degenerative diseases, infections, metabolic disorders, immunologic disorders, disorders of blood vessels, and physical injury.

Genetic disorders are diagnosed by doing a DNA analysis of the individual. They can be treated using traditional methods or gene therapy.

Stress, Anxiety, Bi Polar Disorder, Mental Illness are the mental disorders can be treated with medical marijuana

The study of the endocrine (hormonal) system. This covers growth, hormonal disorders, metabolic bone disorders, amoungst other things.

Metabolic Screening is done to test for congenital genetic disorder in newly born babies by a urine test covering more than 100 metabolic disorders.Metabolic disorders (often called "inborn errors of metabolism") interfere with the body's use of nutrients to maintain healthy tissues and produce energy.In general, metabolic disorders can hinder an infant's normal physical and mental development in a variety of ways. And parents can pass along the gene for a certain disorder without even knowing that they're carriers.

diagnosis of metabolic or systemic diseases that affect kidney function, endocrine disorders, diseases or disorders of the kidneys or urinary tract

Atrial fibrillation and flutter and Wolff-Parkinson-White syndrome are two of the most common disorders treated with catheter ablation.

Minor sleep disorders can be treated with over the counter sleep aids, but more serious disorders are treatable with melatonin.

Major depressive and dysthymic disorders are typically treated with antidepressants or psychosocial therapy.

many genetic disorders cant be treated and the best thing to do is see a genetic councelor or do one of the many things you love to do. but, also some are treatable

Anxiety disorders may be treated in many different ways. Some of these ways are exercise, yoga, therapy, medication, stress and relaxation techniques.

Garfield G. Duncan has written: 'Duncan's Diseases of metabolism' -- subject(s): Metabolism, Disorders 'Diseases of metabolism' -- subject(s): Metabolism, Disorders, Metabolic Diseases 'Diseases of metabolism' -- subject(s): Metabolic Diseases

due to some disease or metabolic disorders there will be a erosion in cardiac that is called as cardiac erosion

Digestive system disorders that include problems related to your GI tract comprising from your mouth to anus are best treated by the medical professional -gastroenterologist in Delhi.

Metabolic Disorders like any other infections (cough or cold) are not contagious. However, if the parents are carriers of a defective gene, then there is a high possibility that the disorder may be passed on to more than one child in that family. They are not passed on to each other between siblings. Sometime it might look like that as the disease shows signs and symptoms at various ages. Metabolic disorders are caused by a defective gene leading to faulty enzyme function which is important for metabolism of food component. In this case as the baby grows with faulty metabolism certain compounds gets accumulated in the body leading to abnormal growth and learning pattern. Metabolic disorders are diagnosed by urine test after birth which acts as a preventive cover for 100 disorders. Early diagnosis leads to early management of the disorders.

A urine based test for genetic metabolic disorder screening is done for baby. It diagnoses babies accurately suffering from any genetic metabolic disorder. Since a healthy, functioning metabolism is crucial for life, metabolic disorders are treated very seriously. A broad range of conditions including PKU and MSUDe are classified as metabolic disorders. However not all can be diagnosed and not all have treatment options available. But for few common ones their is hope. Diagnosing a metabolic disorder can be difficult, as a wide variety of problems create similar symptoms; many patients end up enduring a battery of tests and seeing multiple experts before the root cause of their problems is identified. Simple and safe option is urine based screening for more than 100 disorder. It is non invasive, painless and reliable.

Vitex is another herb recommended for a variety of menstrual disorders ranging from menorrhagia to PMS.

When it comes to genetic metabolic disorders early detection is the prevention of disease manifestation. You can not prevent a genetic disorder from occurring. Screening at birth by painless urine test can prevent the disease from harming the baby. Metabolic disorders are due to a defect in metabolic pathway as the enzyme catalyzing is defective due to a defect in a gene coding it. This situation can not be corrected but can be effectively managed by diet modifications and special foods. Genetic metabolic disorders are not preventable as they are defective gene that are passed from the parents to their offspring, that why screening at birth for these disorders become important. The parents just carry these genes without showing any signs of the disorders which then becomes evident in the baby after birth. Screening through urine sample for more than 100 metabolic disorders is gaining popularity, which is baby friendly rather than pricking them at the heel. Management of these disorders after screening will help in preventing any irreversible damage to the baby. After about 6 months of my baby's birth, my baby started becoming lethargic and less enthusiastic about feeding or even playing. She only slept all the times. Initially, I did not get too concerned about it, as most babies sleep all the time, but then when I showed her to the ped., he immediately asked me to do a metabolic urine test for 100 disorders, which showed positive and then only after modified diet, did my baby start to thrive. If I had known of this test before and that it could be done at birth, I would have not lost so much of time. While my baby is doing well now, I will always regret the fact that I did not do the urine test at birth. While metabolic disorders are not preventible, doing the simple urine test at birth can save a lot of time and pain for the health of the child.

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