Alkaptonuria: Accumulation of the acid in the body due to an enzyme deficiency, leading to dark-colored urine. Other health issues: It may be associated with tissue problems, such as arthritis or skin pigmentation. Monitoring disease progression: Helps evaluate treatment effectiveness and the need for medical interventions.

Individuals with dark urine symptoms: Such as urine turning dark, which may indicate Alkaptonuria. People with a family history of the disorder: Especially if there are hereditary cases of similar conditions. Patients with joint pain: Acid accumulation in tissues can lead to arthritis. Individuals with unusual skin pigmentation: Such as dark spots on the skin. Children showing similar symptoms: Test results can aid in early diagnosis of genetic conditions.

Dark urine: Appearance of dark or black urine, especially when exposed to air. Joint pain: Pain or inflammation in joints, particularly in the spine or major joints. Skin pigmentation: Dark spots on the skin, especially in areas of friction. Fatigue and tiredness: General feeling of tiredness, possibly linked to other health issues. Movement problems: Difficulty or stiffness in joints, which may affect mobility.

What is Homogentisic Acid? It is an intermediate product in metabolism and can accumulate in the body due to genetic disorders. Why is Homogentisic Acid Analysis performed? To diagnose "Black Urine" (Alkaptonuria) and monitor its effects on health. How is the test performed? It requires a urine sample, and you may be asked to collect urine over 24 hours. What are the normal levels of Homogentisic Acid? Normal levels are low, and any increase may indicate a health problem. What factors can affect test results? These include diet, medications, and certain health conditions. What are the next steps if levels are elevated? They may include dietary changes or treatments to monitor the condition. Are there any risks in performing this test? The test is generally safe, but minor risks may include sample collection.

Usually low, with slight variations between laboratories. Generally, less than 1.5 mg/24 hours (approximately 0.1 mg/mL). Any increase may indicate "Black Urine" (Alkaptonuria) or other metabolic disorders. It is always important to consult a doctor for accurate interpretation and next steps.

Homogentisic Acid Test (HGA) | Lahalak Medical Platform

An innovative test precisely measuring homogentisic acid levels to diagnose metabolic disorders like Alkaptonuria, supporting overall health through accurate monitoring.

Prices starts from: 244.12 SAR

Scientific name: Homogentisic Acid Analysis (HPLC)

Homogentisic Acid analysis using High-Performance Liquid Chromatography (HPLC) is a test used to determine the levels of this acid in biological samples, such as urine. This test is important in diagnosing "black urine disease" (Alkaptonuria), a genetic disorder that affects metabolism and leads to the accumulation of the acid in the body. Elevated...

Homogentisic Acid Analysis (HPLC) - Optimal Metabolism Insight

Service type Laboratory test (Urine)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 244.12 SAR

Included Services

Homogentisic Acid Analysis (High-Performance Liquid Chromatography - HPLC) Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Alkaptonuria: Accumulation of the acid in the body due to an enzyme deficiency, leading to dark-colored urine.
Other health issues: It may be associated with tissue problems, such as arthritis or skin pigmentation.
Monitoring disease progression: Helps evaluate treatment effectiveness and the need for medical interventions.

Recommended groups

Individuals with dark urine symptoms: Such as urine turning dark, which may indicate Alkaptonuria.
People with a family history of the disorder: Especially if there are hereditary cases of similar conditions.
Patients with joint pain: Acid accumulation in tissues can lead to arthritis.
Individuals with unusual skin pigmentation: Such as dark spots on the skin.
Children showing similar symptoms: Test results can aid in early diagnosis of genetic conditions.

Symptoms indicative

Dark urine: Appearance of dark or black urine, especially when exposed to air.
Joint pain: Pain or inflammation in joints, particularly in the spine or major joints.
Skin pigmentation: Dark spots on the skin, especially in areas of friction.
Fatigue and tiredness: General feeling of tiredness, possibly linked to other health issues.
Movement problems: Difficulty or stiffness in joints, which may affect mobility.

FAQs

What is Homogentisic Acid? It is an intermediate product in metabolism and can accumulate in the body due to genetic disorders.
Why is Homogentisic Acid Analysis performed? To diagnose "Black Urine" (Alkaptonuria) and monitor its effects on health.
How is the test performed? It requires a urine sample, and you may be asked to collect urine over 24 hours.
What are the normal levels of Homogentisic Acid? Normal levels are low, and any increase may indicate a health problem.
What factors can affect test results? These include diet, medications, and certain health conditions.
What are the next steps if levels are elevated? They may include dietary changes or treatments to monitor the condition.

Normal Levels

Usually low, with slight variations between laboratories.
Generally, less than 1.5 mg/24 hours (approximately 0.1 mg/mL).
Any increase may indicate "Black Urine" (Alkaptonuria) or other metabolic disorders.
It is always important to consult a doctor for accurate interpretation and next steps.