Tyrosine levels: Elevated levels indicate a disruption in its metabolism. Fumaric acid levels: These may be elevated, suggesting a deterioration in the metabolic pathway. Presence of toxic substances: Such as succinylacetone, which is attributed to a deficiency in enzymes needed to break down tyrosine.

Newborns: Especially if they show symptoms suggesting metabolic disorders, such as frequent vomiting or growth problems. Children with a family history: If there are previous cases of Tyrosinemia in the family. Individuals showing symptoms: Such as abdominal pain, jaundice, or symptoms of liver damage. Patients being evaluated for unexplained health issues: When a metabolic disorder is suspected.

Frequent vomiting: Especially after eating. Diarrhea: Frequent and unexplained. Weight loss: Or difficulty gaining weight. Jaundice: Yellowing of the skin and eyes. Abdominal pain: Especially in the liver area. Growth delay: Or issues with mental and physical development. Severe fatigue: Or unexplained weakness.

What is the purpose of this test? To diagnose a metabolic disorder that affects tyrosine metabolism. How is the test performed? It is done by collecting blood and urine samples. Does the test require fasting? You may be asked to fast for a certain period before the test. What is the waiting period for results? It usually takes a few days to a week. What are the treatment options if the result is positive? Treatment may include a special diet and medications to reduce tyrosine levels. Are there any side effects of the test? The patient may feel some discomfort during the blood draw, but other side effects are rare.

Tyrosine levels in the blood: Considered normal if less than 0.2 mg/dL. Fumaric acid levels: Should be within the normal range, typically less than 0.5 mg/dL. Presence of other metabolic products: Such as succinylacetone, which should also be within normal limits.

Tyrosinemia Type 1 Screening | Lahalak Platform

Specialized screening for early detection of hereditary tyrosinemia in infants, ensuring prompt medical intervention to protect the liver and kidneys from serious long-term complications.

Prices starts from: 443.62 SAR

Scientific name: Tyrosinemia Type 1 Screening Test

The Tyrosinemia Type 1 analysis is a specialized test used to diagnose a rare genetic disorder that affects the metabolism of tyrosine, leading to the accumulation of toxic acids in the body. The test measures levels of tyrosine and other amino acids in blood or urine samples, providing precise information about metabolic function. This test is pri...

Tyrosinemia Type 1 Screening Test - Newborn Tyrosinemia Screening

Service type Laboratory test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 443.62 SAR

Included Services

Tyrosinemia Type 1Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Tyrosine levels: Elevated levels indicate a disruption in its metabolism.
Fumaric acid levels: These may be elevated, suggesting a deterioration in the metabolic pathway.
Presence of toxic substances: Such as succinylacetone, which is attributed to a deficiency in enzymes needed to break down tyrosine.

Recommended groups

Newborns: Especially if they show symptoms suggesting metabolic disorders, such as frequent vomiting or growth problems.
Children with a family history: If there are previous cases of Tyrosinemia in the family.
Individuals showing symptoms: Such as abdominal pain, jaundice, or symptoms of liver damage.
Patients being evaluated for unexplained health issues: When a metabolic disorder is suspected.

Symptoms indicative

Frequent vomiting: Especially after eating.
Diarrhea: Frequent and unexplained.
Weight loss: Or difficulty gaining weight.
Jaundice: Yellowing of the skin and eyes.
Abdominal pain: Especially in the liver area.
Growth delay: Or issues with mental and physical development.

FAQs

What is the purpose of this test? To diagnose a metabolic disorder that affects tyrosine metabolism.
How is the test performed? It is done by collecting blood and urine samples.
Does the test require fasting? You may be asked to fast for a certain period before the test.
What is the waiting period for results? It usually takes a few days to a week.
What are the treatment options if the result is positive? Treatment may include a special diet and medications to reduce tyrosine levels.
Are there any side effects of the test? The patient may feel some discomfort during the blood draw, but other side effects are rare.

Normal Levels

Tyrosine levels in the blood: Considered normal if less than 0.2 mg/dL.
Fumaric acid levels: Should be within the normal range, typically less than 0.5 mg/dL.
Presence of other metabolic products: Such as succinylacetone, which should also be within normal limits.

Conditions & Notices

The terms and conditions announced on the "Lahalak" medical platform apply.
There are no special conditions for the service other than those mentioned.

Tyrosinemia Type 1 Screening | Lahalak Platform

Included Services

Medical Service Information

Purpose Test

Recommended groups

Symptoms indicative

FAQs

Normal Levels

Conditions & Notices

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