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Test Price

600 AED

✅ Home Collection Available

ATRX Immunohistochemistry (IHC) Test in UAE | 600 AED | DHA Licensed

Executive Summary & Core Metrics

ATRX Immunohistochemistry (IHC) Test – 99.9% diagnostic sensitivity for glioma characterization and sarcoma profiling. Secure medical courier solid tissue specimen retrieval via ISO-certified cold chain logistics (available daily from 8 AM to 11 PM). Includes telephonic post-test clinical guidance from a DHA-licensed consultant and direct billing verification via WhatsApp at +971 54 548 8731. Full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.

Test Overview & Methodology

The ATRX Immunohistochemistry (IHC) test detects loss of the ATRX nuclear protein in formalin‑fixed, paraffin‑embedded (FFPE) tumour tissue, a hallmark of IDH‑mutant astrocytomas and certain sarcomas. Delivering results within 5–7 working days, this accredited assay enables oncologists and surgical pathologists to refine diagnosis and tailor molecularly guided therapy under DHA oncology protocols.

Feature Our ATRX IHC Test Closest Alternative
Methodology High‑sensitivity monoclonal IHC with internal validation & DAB chromogen Standard IHC with polyclonal antibody, variable sensitivity
ISO Accreditation ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) May lack current ISO certification for immunohistochemistry
Turnaround Time 5 working days (block) / 5–7 days (complex tissue) Often 7–10 days; no expedited processing
Home Collection & Logistics Secure medical courier solid tissue specimen retrieval; cold‑chain FFPE transport (8 AM–11 PM) Standard drop‑off; no guaranteed temperature‑controlled pickup
Price (AED) 600 650 – 800
Post‑Test Support Telephonic clinical guidance by DHA‑licensed consultant Report only; no result interpretation service

Physician Insight & Safety Protocols

A Note from Mr. Prabhakar Reddy Kalathoor (DHA Registration ID: 61713011)

“As a specialist in diagnostic radiology, I understand the need for precise molecular characterization in oncology. An ATRX IHC result provides critical data for accurate tumour subtyping. This information should be integrated with full clinical and imaging assessments for optimal patient management.”

Patient Advisory & Preparation

Important Notice

Secure medical courier solid tissue specimen retrieval is arranged for FFPE blocks or prepared pathology slides. Ensure original histopathology reports and clinical history accompany the sample. Do not alter any prescribed medications without prior consultation with your treating oncologist.

Patient Safety Exclusion Criteria & Emergency Red Flags

  • Exclusion: Insufficient or improperly fixed tissue sample; lack of original histopathology report, biopsy site details, or complete clinical history.
  • Exclusion: Samples not submitted in 10% formal‑saline or standard FFPE block; frozen specimens require prior lab approval.
  • Red Flag: New or worsening neurological symptoms (seizures, sudden vision loss, confusion) — seek emergency care immediately.
  • Red Flag: Uncontrolled pain, bleeding, or swelling at the biopsy site — contact your surgical team or visit the nearest ER.

Always provide the required clinical documentation. This test is intended for patients with a confirmed or suspected solid tumour under the care of a licensed oncologist or surgical pathologist.

Patient FAQ & Clinical Guidance

1. Why is ATRX testing recommended for glioma patients?

ATRX loss identifies IDH‑mutant astrocytomas and distinguishes them from oligodendrogliomas, enabling oncologists to select targeted therapies and avoid ineffective treatments. This immunohistochemical marker is a cornerstone of the WHO CNS tumour classification and directly influences prognosis.

2. What does a positive (loss) ATRX result mean?

A positive ATRX loss result indicates a diagnosis of IDH‑mutant astrocytoma, generally associated with a more favourable prognosis than ATRX‑retained wild‑type gliomas. This finding helps oncologists tailor follow‑up imaging, adjuvant therapy, and genetic counselling where appropriate.

3. How is the sample collected?

A tissue biopsy is performed at an accredited hospital by your surgeon. Our secure medical courier service retrieves the prepared FFPE block or formalin‑fixed specimen, available daily from 8 AM to 11 PM. Simply provide the histopathology report, biopsy site, and clinical history for accurate processing.

4. What is the turnaround time for results?

Results are typically available within 5 working days for standard FFPE blocks. Complex tissue specimens may require 5–7 days. You will receive a detailed report including immunohistochemical interpretation.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE operates under DHA Facility License Number 1143 and is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139). All patient data is securely handled in accordance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name ATRX Immunohistochemistry (IHC)
Price (AED) 600
Turnaround Time 5–7 working days
Sample Type / Matrix Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block or Biopsy Slides
Methodology Used Monoclonal Immunohistochemistry (IHC) with DAB chromogen
ICD-10-CM Code C71.9 (Malignant neoplasm of brain, unspecified)
LOINC Code 100667-0 (ATRX gene rearrangement in Tissue by FISH)
DHA Facility License 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE

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