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Amino Acid Disorder Gene Panel / Maple Syrup Urine Disease (MSUD) Panel

Also known as: Maple syrup urine disease Gene Panel by NGS, EDTA Blood**

50+ booked in last 3 days

Maple syrup urine disease Gene Panel by NGS, EDTA Blood** Details in Brief

Also Known As Maple syrup urine disease Gene Panel by NGS
Purpose To detect genetic mutations causing maple syrup urine disease and support diagnosis, management, and family screening
Preparation No special preparation required
Fasting Fasting not required
Reporting Time After 4 weeks
Cost 19,400

Overview

What is the Amino Acid Disorder Gene Panel / MSUD Panel?

The Amino Acid Disorder Gene Panel, also known as the Maple Syrup Urine Disease panel, is a genetic blood test used to diagnose MSUD. MSUD is a rare inherited metabolic condition in which the body is unable to properly break down certain amino acids, namely leucine, isoleucine, and valine.

This test analyses multiple genes involved in branched chain amino acid metabolism using Next Generation Sequencing technology. It requires an EDTA blood sample and helps doctors confirm the diagnosis, guide treatment decisions, and assess genetic risk for family members.

What Does the Amino Acid Disorder Gene Panel / MSUD Panel Measure?

This genetic test evaluates changes in genes responsible for amino acid breakdown and energy metabolism:

  • Detection of disease causing variants linked to maple syrup urine disease
  • Differentiation of MSUD from other metabolic encephalopathies
  • Identification of inherited risk for metabolic crises during illness or fasting
  • Support for long term dietary planning and treatment strategies
  • Guidance for genetic counselling, family screening, and prenatal evaluation

Amino Acid Disorder Gene Panel / MSUD Panel: Who Needs It and Why It’s Done

What Symptoms May Call for an Amino Acid Disorder Gene Panel / MSUD Panel?

Doctors may recommend this test if you or your child experience symptoms such as:

  • Poor feeding, vomiting, or lethargy in newborns
  • Developmental delay or regression
  • Seizures or abnormal muscle tone
  • Episodes of altered consciousness or coma
  • A characteristic sweet or maple syrup like odour in urine

Who Should Get an Amino Acid Disorder Gene Panel / MSUD Panel?

  • Newborns with abnormal metabolic screening results
  • Infants or children with suspected inherited amino acid disorders
  • Individuals with recurrent unexplained metabolic crises
  • Patients with a family history of maple syrup urine disease
  • Couples planning a pregnancy with known genetic risk

Why is an Amino Acid Disorder Gene Panel / MSUD Panel Done?

The test helps confirm the genetic cause of maple syrup urine disease, enabling early treatment, prevention of life threatening metabolic episodes, and informed family planning.

Importance of the Amino Acid Disorder Gene Panel / MSUD Panel

Early diagnosis of MSUD is critical because untreated disease can lead to severe neurological damage or death. This gene panel allows precise identification of the underlying genetic defect, helping your doctor initiate timely dietary management, monitor metabolic stability, and reduce the risk of acute metabolic decompensation. It also supports long term care planning and family counselling.

Amino Acid Disorder Gene Panel / MSUD Panel Booking & Reports – Metropolis Healthcare

How to Book the Amino Acid Disorder Gene Panel / MSUD Panel and Get Your Reports?

  1. Simple Online Booking
    Booking can be done through the Metropolis Healthcare App or website. Select the Amino Acid Disorder Gene Panel or MSUD Panel, choose a convenient time slot, and provide your address for a blood test at home. You may also visit a nearby Metropolis Lab if you prefer in person sample collection.
  2. Safe Home Sample Collection
    Trained phlebotomists collect your blood sample while strictly following safety and hygiene protocols.
  3. Sample Tracking Updates
    You receive updates at every stage, from sample collection to testing, through the Metropolis Healthcare platform.
  4. Accurate Laboratory Testing
    Your sample is processed at NABL and CAP accredited laboratories using advanced molecular diagnostic technology.
  5. Quick and Easy Reports
    Your reports are shared via email, WhatsApp, or can be downloaded from the Metropolis Healthcare website or app.

Is Home Sample Collection for Amino Acid Disorder Gene Panel / MSUD Panel Available Near You?

Yes, Metropolis Healthcare offers home sample collection for the Amino Acid Disorder Gene Panel or MSUD Panel. This service saves you time, reduces the need for travel, and ensures professional sample handling while maintaining strict quality standards.

How Long Does It Take to Get an Amino Acid Disorder Gene Panel / MSUD Panel Report?

Reports are usually available after 4 weeks once the sample reaches the lab.
Note: Reporting time may vary based on your location.

Where Can I See or Get Amino Acid Disorder Gene Panel / MSUD Panel Results?

  1. Metropolis Healthcare website or mobile app
    You can access your test results through the Metropolis Healthcare website or mobile app using your login credentials.
  2. Email or WhatsApp
    Reports are also shared via email or WhatsApp.
  3. Physical copy from the lab
    You may collect a physical copy directly from the Metropolis Lab if required.

Interpreting Amino Acid Disorder Gene Panel / MSUD Panel Results

What Your Amino Acid Disorder Gene Panel / MSUD Panel Results May Indicate

Parameter Expected Finding Pathogenic Variant Detected May Indicate No Variant Detected May Indicate
MSUD related genes No disease causing variant detected Maple syrup urine disease affecting branched chain amino acid metabolism Symptoms may be due to other metabolic or genetic conditions

Understanding Abnormal Amino Acid Disorder Gene Panel / MSUD Panel Test Results

Gene Group What a Pathogenic Variant May Indicate
BCKDHA and BCKDHB Classic MSUD due to defective branched chain ketoacid dehydrogenase
DBT Intermediate or variant forms of MSUD
DLD MSUD with additional mitochondrial or neurological involvement
PPM1K Impaired regulation of amino acid metabolism and energy production

How Should You Prepare for an Amino Acid Disorder Gene Panel / MSUD Panel?

This genetic test requires minimal preparation. Please keep the following points in mind:

  • No fasting required: You can eat and drink normally unless advised otherwise by your doctor
  • Normal hydration: Continue your usual fluid intake
  • Medication information: Inform your doctor about all medicines or supplements you are taking
  • Clinical history: Share relevant medical and family history to support accurate interpretation
  • Consent and forms: Ensure the test requisition form and genetic history details are completed

How Is an Amino Acid Disorder Gene Panel / MSUD Panel Done? (Step-by-Step Procedure)

The test is performed using a simple blood collection process:

  • Preparation: A tourniquet is tied around your arm to make veins more visible.
  • Cleaning: The puncture site is cleaned with antiseptic.
  • Sample Collection: A sterile needle is used to draw about 3 to 5 ml of blood into an EDTA vacutainer.
  • Completion: The needle is removed, and a bandage is applied.
  • Processing: The sample is analysed using Next Generation Sequencing to identify gene mutations linked to maple syrup urine disease.

Conditions That May Affect Amino Acid Disorder Gene Panel / MSUD Panel Accuracy

Certain patient related factors may influence test interpretation:

  • Recent blood transfusion may affect genetic analysis
  • Incomplete or incorrect clinical history can limit interpretation
  • Mosaic genetic changes may be harder to detect in some individuals
  • Variants of uncertain significance may require further family testing

Diseases That an Amino Acid Disorder Gene Panel / MSUD Panel Can Help Detect

  • Maple syrup urine disease
  • Branched chain amino acid metabolism disorders
  • Inherited metabolic encephalopathies

References

  1. Chuang D.T., Shih V.E., Max Wynn R. (2006). Maple syrup urine disease (branched chain ketoacid dehydrogenase deficiency). Current Molecular Medicine, 6(5), 537–546. PMID: 16918370
  2. Strauss K.A., Puffenberger E.G., Robinson D.L., Morton D.H. (2009). Type I maple syrup urine disease: A model metabolic disorder. Molecular Genetics and Metabolism, 98(1–2), 3–11. PMID: 19608456
  3. Simon E., Fingerhut R., Baumkötter J., et al. (2006). Maple syrup urine disease: Favourable effect of early diagnosis by newborn screening on the neonatal course of the disease. Journal of Inherited Metabolic Disease, 29(4), 532–537. PMID: 16972195
  4. Nellis M.M., Danner D.J. (2001). Gene preference in maple syrup urine disease. American Journal of Human Genetics, 68(1), 232–237. PMID: 11085915
  5. Zinnanti W.J., Lazovic J., Griffin K., et al. (2009). Dual mechanism of brain injury and novel treatment strategy in maple syrup urine disease. Brain, 132(4), 903–918. PMID: 19286687
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Maple syrup urine disease Gene Panel by NGS, EDTA Blood** Price

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Maple syrup urine disease Gene Panel by NGS, EDTA Blood** with a clear pricing structure.

The Maple syrup urine disease Gene Panel by NGS, EDTA Blood** Price in Ahmedabad is ₹ 19,400 .

We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.

Frequently Asked Questions

This test can be done at any time of the day, as it does not depend on fasting or daily body rhythms.
No fasting is required. You can eat and drink normally before the blood sample is collected.
Dehydration does not affect genetic results, but staying well hydrated helps ensure smooth blood collection.
No special diet changes are needed. Inform your doctor about all medicines or supplements you are taking.
A trained professional collects a small blood sample from a vein in your arm using sterile techniques.
Are there any risks to the test?
A normal result means no disease causing genetic variants were detected, though results should always be interpreted alongside clinical findings.
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