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Duchene Muscular Dystrophy (DMD)
Duchene Muscular Dystrophy (DMD)
Duchenne muscular dystrophy (DMD) is one of the most severe forms of inherited muscular dystrophies. Mutations in the dystrophin gene lead to progressive muscle fiber degeneration and weakness. It is an X-linked recessive disorder where males are affected but females are unaffected carriers. The test analyses 72 exonic gene deletions and duplications to diagnose DMD or the carrier status in female.
15000
₹2599
76% OFF
2 weeks
Schedule test now
Schedule test now
Sample Collection and Transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
DMD, Duchene Muscular Dystrophy, Beckers Muscular Dystrophy, Carrier Screening for DMD
Specialities
ObGyn, Pediatricians, Neonatologists
Technology
Deletions and duplications of 72 exons in Dystrophin gene are detected by MLPA technology. Multiplex ligation-dependent probe amplification (MLPA) uses pairs of probes to detect specific sections of the genome. It is mainly used to identify exon-level copy number variation.
Conditions & Symptoms
Family history of DMD, DMD Clinical phenotype
Additional Information
GeneTech pioneered genetic testing in India in 1998 and has the most comprehensive range of tests using technologies.
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Test CatalogueDuchene Muscular Dystrophy (DMD)

Full Body Checkup - Essential in Hyderabad

Unlock insights into your health, ancestry, or future risks with our advanced genetic testing. Backed by cutting-edge science and expert guidance, Genetech helps you make informed decisions—personalized to your DNA.

₹1599
₹2599
76% OFF
2 weeks
Schedule test now

Duchene Muscular Dystrophy (DMD)

Duchenne muscular dystrophy (DMD) is one of the most severe forms of inherited muscular dystrophies. Mutations in the dystrophin gene lead to progressive muscle fiber degeneration and weakness. It is an X-linked recessive disorder where males are affected but females are unaffected carriers. The test analyses 72 exonic gene deletions and duplications to diagnose DMD or the carrier status in female.

15000
₹2599
76% OFF
3 weeks
Schedule test now
Sample collection and transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
DMD, Duchene Muscular Dystrophy, Beckers Muscular Dystrophy, Carrier Screening for DMD
Specialities
ObGyn, Pediatricians, Neonatologists
Technology
Deletions and duplications of 72 exons in Dystrophin gene are detected by MLPA technology. Multiplex ligation-dependent probe amplification (MLPA) uses pairs of probes to detect specific sections of the genome. It is mainly used to identify exon-level copy number variation.
Conditions & Symptoms
Family history of DMD, DMD Clinical phenotype
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Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
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Amniocentesis
Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy. Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid from the womb. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
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GeneTech is India’s leading genetics testing laboratory with the most comprehensive directory of genetic tests. We were established in Hyderabad in 1998, and have operations all over India.
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Book Counselling

GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.
GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.

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