Test Price
2,800 AED✅ Home Collection Available
NIN Gene Seckel Syndrome Type 7 (SCKL7) Genetic Test in UAE | DNA Labs UAE
Executive Summary & Core Metrics
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily 8 AM – 11 PM).
- ✓ Clinical Guidance: Post-Test Genetic Counseling Session Included.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- ✓ Price: 2,800 AED (All-Inclusive).
Test Overview & Methodology
This NGS-based DNA analysis targets the NIN gene, the primary cause of Seckel syndrome type 7 (SCKL7)—a rare autosomal recessive disorder marked by severe microcephaly, proportionate dwarfism, and distinctive craniofacial features. Early molecular confirmation empowers families with a definitive diagnosis and guides multidisciplinary care.
| Feature | DNA Labs UAE Test | Closest Alternative |
|---|---|---|
| Methodology | Next-Generation Sequencing (Illumina NovaSeq X Plus) | Sanger Sequencing |
| Precision / Sensitivity | 99.9% Diagnostic Sensitivity | ~95% |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Price (AED) | 2,800 | 3,500 |
| Home Collection | Included (VIP Mobile Phlebotomy) | Not Available |
Physician Insight & Safety Protocols
"Diagnosing a rare genetic condition like Seckel syndrome type 7 requires not only advanced molecular technology but also a deep understanding of its clinical presentation. The NIN gene analysis provides a crucial piece of the diagnostic puzzle, which must be interpreted alongside thorough clinical evaluation and familial history. Our commitment at DNA Labs UAE is to deliver accurate, timely results and provide compassionate post-test counseling to support families in their next steps."
— Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Medication Advisory & Patient Safety
Medication Warning: Do not discontinue, alter, or start any prescribed medication without consulting your treating physician. This genetic test result should be reviewed with your healthcare provider to inform any therapeutic decisions.
Exclusion Criteria & Red Flags
Exclusion Criteria for Home Collection
- Active febrile illness requiring immediate medical attention
- Known severe bleeding disorders unmanaged
- Lack of informed consent or legal guardian authorisation for minors
- Patients in clinically unstable condition
Emergency Red Flags
- New-onset seizures or loss of consciousness
- Rapidly increasing head circumference or signs of raised intracranial pressure
- Apnoea or severe respiratory distress in infants
- Suspected abuse or neglect alongside dysmorphic features
Patient FAQ & Clinical Guidance
1. What is the NIN gene Seckel syndrome type 7 test?
This next-generation sequencing test comprehensively analyses the NIN gene for pathogenic variants linked to Seckel syndrome type 7 with 99.9% clinical sensitivity. It detects single nucleotide variants, small insertions/deletions, and copy number variations, providing a definitive molecular diagnosis when correlated with clinical features.
2. How accurate is this genetic test?
Our NGS-based assay achieves a 99.9% diagnostic sensitivity for the NIN gene, effectively identifying the vast majority of known pathogenic mutations causing Seckel syndrome type 7. Rare deep intronic or epigenetic variants may require additional methods, but a negative result significantly reduces the likelihood of this specific subtype.
3. What does the 2,800 AED price include?
The all-inclusive fee covers VIP mobile phlebotomy for home collection, temperature-controlled cold-chain transport, a genetic counseling session, laboratory processing via NGS, and a detailed clinical report. Prior to sample collection, our team verifies your insurance coverage directly via WhatsApp at +971 54 548 8731 and assists with approvals from major UAE insurers.
4. How is the sample collected?
A certified mobile phlebotomist visits your home to perform a standard peripheral blood draw using hospital-grade protocols. The sample is transported under strict cold-chain conditions to our ISO 9001:2015 accredited laboratory in Dubai Healthcare City.
5. When will I receive the results?
The standard turnaround time is 3 to 4 weeks from sample collection. You will receive a comprehensive clinical report along with a post-test genetic counseling session to discuss the findings and their implications for patient management.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE strictly complies with the following UAE federal legislations governing medical data, genetic testing, and patient privacy:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Federal Decree-Law No. 4 of 2016 on Medical Liability.
All genetic data is encrypted, access-controlled, and processed under strict confidentiality agreements. Informed consent is obtained prior to sample collection and analysis.
Clinical & Logistical Metadata
| Test Name | NIN Gene Seckel Syndrome Type 7 (SCKL7) Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 Weeks (21–28 Days) |
| Sample Type / Matrix | Whole Blood (Peripheral) |
| Methodology Used | Next-Generation Sequencing (NGS) – Illumina NovaSeq X Plus |
| ICD-10-CM Code | Q87.1 |
| LOINC Code | 82307-8 |
| DHA Facility License & Laboratory Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians