CPEO (CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA) DETECTION / EDTA BLOOD

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NABL Cap Accredited 
The CPEO Detection EDTA Blood test identifies genetic or mitochondrial abnormalities associated with Chronic Progressive External Ophthalmoplegia, a condition causing gradual eye muscle weakness. Metropolis Healthcare performs this test using advanced molecular diagnostic techniques to ensure accurate detection of underlying mutations. It assists clinicians in confirming diagnosis, understanding disease progression, and planning management strategies. When interpreted with clinical evaluation and imaging, it offers valuable insight into this rare neuromuscular disorder.

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Price: Rs. 7,560.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: C0256

Frequently Asked Questions (FAQ's):

What does the CPEO detection test include at Metropolis Healthcare?
It includes molecular analysis of blood to detect genetic or mitochondrial alterations linked to CPEO.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses validated molecular diagnostics and strict quality protocols for precise mutation detection.

Why is this test important?
It helps confirm diagnosis and differentiate CPEO from other neuromuscular or ophthalmic conditions.

Who should take this test at Metropolis Healthcare?
Patients with progressive eye muscle weakness, ptosis, or suspected mitochondrial disorders.

Do I need special preparation before the test?
No special preparation is required; an EDTA blood sample is sufficient.

How can results help clinicians at Metropolis Healthcare?
Results guide diagnosis, genetic counselling, and long-term management planning.

Can this test identify all causes of ophthalmoplegia?
It identifies known genetic or mitochondrial causes; Metropolis Healthcare interprets results along with clinical findings.

When will I receive my results from Metropolis Healthcare?
Results are provided within the standard turnaround time for molecular testing.

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