Primarily used to diagnose and monitor certain genetic disorders, such as: Niemann-Pick disease: Low enzyme levels may indicate the presence of the disease. Other metabolic disorders: Affect how the body processes sulfur-containing compounds. Niemann-Pick disease: Low enzyme levels may indicate the presence of the disease. Other metabolic disorders: Affect how the body processes sulfur-containing compounds.

Individuals with symptoms of Niemann-Pick disease: such as neurological problems or developmental delays. People with a family history: in cases of inherited metabolic disorders. Children: who show unexplained signs or symptoms related to growth or the nervous system. Adults: experiencing unexplained health issues that may be linked to metabolic disorders.

Growth delay: difficulties in physical or mental development in children. Neurological problems: such as muscle weakness, loss of balance, or coordination difficulties. Psychological symptoms: changes in behavior, anxiety, or depression. Movement changes: such as tremors or involuntary movements. Vision problems: such as vision loss or visual disturbances.

What is the purpose of the Arylsulfatase A test? It is used to assess Arylsulfatase A enzyme levels to diagnose genetic disorders such as Niemann-Pick disease. How is the sample collected? Urine is collected over 24 hours in a designated container. Does the test require any preparation? Usually not, but avoiding certain medications or supplements may be recommended before the test. How long does it take to get results? Varies by laboratory, but results are typically available within a few days. What do high or low results mean? Low levels: May indicate enzyme deficiency, requiring further tests for diagnosis. High levels: Generally considered within the normal range, but should be interpreted by a doctor. Low levels: May indicate enzyme deficiency, requiring further tests for diagnosis. High levels: Generally considered within the normal range, but should be interpreted by a doctor. Can diet affect the results? Generally minimal, but it is best to follow laboratory instructions. What are the next steps if the results are positive? Consult a specialist to determine a treatment plan or further testing. Can the test be done for children? Yes, it is recommended for children showing relevant symptoms.

Urine: Arylsulfatase A levels in urine are usually less than 1.5 nmol/hour/mL. Blood Sample: Enzyme levels should ideally be within a specific range, and test results are generally considered acceptable within limits set by the laboratory.

Arylsulfatase A (ASA) Test Price | Lahalak Platform

Accurate evaluation of Arylsulfatase A levels in urine to diagnose rare genetic and metabolic disorders, supporting early and informed treatment decisions.

Prices starts from: 422.4 SAR

Scientific name: Arylsulfatase A (ASA) Test

Arylsulfatase A (ASA) analysis in 24-hour urine is a test used to evaluate the level of the enzyme arylsulfatase A in the body. This enzyme is essential for breaking down sulfur-containing compounds, and the test helps diagnose certain genetic disorders, such as Niemann-Pick disease. A 24-hour urine sample is collected, allowing accurate measuremen...

Arylsulfatase A (ASA) Test - Arylsulfatase A Enzyme Test

Service type Laboratory test (24h Urine)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 422.4 SAR

Included Services

Arylsulfatase A Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Primarily used to diagnose and monitor certain genetic disorders, such as: Niemann-Pick disease: Low enzyme levels may indicate the presence of the disease. Other metabolic disorders: Affect how the body processes sulfur-containing compounds.
Niemann-Pick disease: Low enzyme levels may indicate the presence of the disease.
Other metabolic disorders: Affect how the body processes sulfur-containing compounds.

Recommended groups

Individuals with symptoms of Niemann-Pick disease: such as neurological problems or developmental delays.
People with a family history: in cases of inherited metabolic disorders.
Children: who show unexplained signs or symptoms related to growth or the nervous system.
Adults: experiencing unexplained health issues that may be linked to metabolic disorders.

Symptoms indicative

Growth delay: difficulties in physical or mental development in children.
Neurological problems: such as muscle weakness, loss of balance, or coordination difficulties.
Psychological symptoms: changes in behavior, anxiety, or depression.
Movement changes: such as tremors or involuntary movements.
Vision problems: such as vision loss or visual disturbances.

FAQs

What is the purpose of the Arylsulfatase A test? It is used to assess Arylsulfatase A enzyme levels to diagnose genetic disorders such as Niemann-Pick disease.
How is the sample collected? Urine is collected over 24 hours in a designated container.
Does the test require any preparation? Usually not, but avoiding certain medications or supplements may be recommended before the test.
How long does it take to get results? Varies by laboratory, but results are typically available within a few days.
What do high or low results mean? Low levels: May indicate enzyme deficiency, requiring further tests for diagnosis. High levels: Generally considered within the normal range, but should be interpreted by a doctor.
Low levels: May indicate enzyme deficiency, requiring further tests for diagnosis.

Normal Levels

Urine: Arylsulfatase A levels in urine are usually less than 1.5 nmol/hour/mL.
Blood Sample: Enzyme levels should ideally be within a specific range, and test results are generally considered acceptable within limits set by the laboratory.