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ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Genetic Test

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ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Genetic Test

Short Name: ALG11 CDG Type Ip NGS Test

Also known as: ALG11 CDG Type Ip, Congenital Disorder of Glycosylation Type Ip

ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS) Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To diagnose congenital disorder of glycosylation type Ip caused by mutations in the ALG11 gene using next-generation sequencing technology.

Test Code
1950
Price
₹20,000
Sample Type
Blood or Extracted DNA
Result Time
3 to 4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling to draw a pedigree chart of family members affected with Congenital Disorder of Glycosylation Type Ip.

Method: Blood draw or FTA card

Step 2

Laboratory Analysis

Standard blood draw or FTA card sample collection by a trained professional.

Step 3

Report Delivery

Sample is sent to the laboratory for NGS analysis and genetic counseling may continue post-test.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Provide clinical history and undergo genetic counseling to draw a pedigree chart of family members affected with Congenital Disorder of Glycosylation Type Ip.
2
During the Test:Standard blood draw or FTA card sample collection by a trained professional.
3
After the Test:Sample is sent to the laboratory for NGS analysis and genetic counseling may continue post-test.

About This Test

Who Should Get This Test

To diagnose congenital disorder of glycosylation type Ip caused by mutations in the ALG11 gene using next-generation sequencing technology.

How to Prepare

  • Ensure proper sample handling and labeling.
  • Follow instructions for FTA card if used.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early diagnosis through NGS testing is crucial for managing symptoms and improving quality of life in ALG11 CDG Type Ip."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA
Collection MethodBlood draw or FTA card
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

The test results indicate the presence or absence of pathogenic variants in the ALG11 gene associated with Congenital Disorder of Glycosylation Type Ip.
Positive result: Indicates a pathogenic variant in the ALG11 gene, confirming diagnosis. Clinical correlation and genetic counseling are advised.
Negative result: No pathogenic variants detected. Clinical symptoms may require further investigation.
Variant of uncertain significance: Further testing or family studies may be needed to determine clinical relevance.
⚠️ When to Consult a Doctor:

If symptoms such as developmental delays, seizures, or failure to thrive are present, consult a geneticist or healthcare provider for evaluation and possible testing.

Limitations

  • ⚠Symptoms may overlap with other genetic disorders, complicating diagnosis.

Frequently Asked Questions

What is ALG11 Congenital Disorder of Glycosylation Type Ip?
ALG11 CDG Type Ip is a rare genetic disorder caused by mutations in the ALG11 gene, affecting the body's ability to produce and process glycoproteins, leading to symptoms like developmental delays and neurological problems.
What are the symptoms of ALG11 CDG Type Ip?
Symptoms vary but commonly include developmental delays, neurological issues, seizures, failure to thrive, enlarged liver and spleen, and gastrointestinal problems.
How is ALG11 CDG Type Ip diagnosed?
Diagnosis involves genetic testing, such as NGS for the ALG11 gene, along with clinical evaluation, blood/urine tests, and possibly imaging or biopsies.
What is NGS genetic testing?
Next-generation sequencing (NGS) is a advanced DNA analysis technique that can detect mutations in genes like ALG11 with high accuracy for diagnosing genetic disorders.
What is the cost of the ALG11 Gene NGS Test in India?
The cost is INR 20,000 at DNA Labs India, which includes home sample collection and report delivery.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
How long does it take to get the test results?
Results are typically available in 3 to 4 weeks, delivered via online portal, email, or WhatsApp.
Is the test covered by insurance?
Coverage depends on your insurance policy; it is not universally covered. Check with your provider for details.
Who should consider getting this test?
Individuals with symptoms of CDG Type Ip, those with a family history, or after genetic counseling may consider this test for diagnosis.
What should I do if the test is positive?
A positive result confirms ALG11 CDG Type Ip. Consult a geneticist for management options, supportive care, and family planning advice.
Are there any risks associated with the test?
The test itself has minimal risks, primarily from blood draw (e.g., bruising). Genetic testing may have psychological implications; counseling is recommended.
How can I prepare for the test?
Prepare by providing clinical history, attending genetic counseling, and following sample collection instructions. No fasting is typically required.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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