Short Description

NGS genetic DNA test detecets for variant and mutation detection in CHKB gene for Muscular dystrophy, congenital, megaconial type

PreTest Information

Clinical History of Patient who is going for CHKB Gene Muscular dystrophy, congenital, megaconial type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHKB Gene Muscular dystrophy, congenital, megaconial type

Detail Description

CHKB Gene Muscular Dystrophy, Congenital, Megaconial Type: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Muscular dystrophy is a genetic disorder that affects the muscles and causes them to weaken over time. There are many different types of muscular dystrophy, and one of them is the congenital megaconial type, which is caused by mutations in the CHKB gene. In this blog, we will discuss the symptoms, diagnosis, and NGS genetic DNA test cost for CHKB gene muscular dystrophy, congenital, megaconial type.

Symptoms of CHKB Gene Muscular Dystrophy, Congenital, Megaconial Type

The symptoms of CHKB gene muscular dystrophy, congenital, megaconial type typically begin in early childhood. Some of the most common symptoms include:

• Muscle weakness and wasting
• Poor muscle tone
• Delayed motor development
• Difficulty walking and running
• Difficulty standing up from a seated position
• Difficulty climbing stairs
• Difficulty lifting objects
• Difficulty swallowing
• Heart problems

It is important to note that the symptoms of CHKB gene muscular dystrophy, congenital, megaconial type can vary from person to person. Some people may have mild symptoms, while others may have severe symptoms that affect their daily life.

Diagnosis of CHKB Gene Muscular Dystrophy, Congenital, Megaconial Type

The diagnosis of CHKB gene muscular dystrophy, congenital, megaconial type typically involves a combination of physical examination, medical history, and genetic testing. A doctor may perform a physical examination to check for muscle weakness and wasting, poor muscle tone, and other symptoms. They may also ask about your family history of muscular dystrophy.

Genetic testing is the most reliable way to diagnose CHKB gene muscular dystrophy, congenital, megaconial type. This involves analyzing a blood or saliva sample to look for mutations in the CHKB gene. This type of testing is called Next-Generation Sequencing (NGS) genetic DNA test.

NGS Genetic DNA Test Cost for CHKB Gene Muscular Dystrophy, Congenital, Megaconial Type

The cost of NGS genetic DNA test for CHKB gene muscular dystrophy, congenital, megaconial type in India ranges from INR 15,000 to INR 25,000. The cost may vary depending on the laboratory and location. DNA Labs India is one of the leading genetic testing laboratories in India that offers NGS genetic DNA test for CHKB gene muscular dystrophy, congenital, megaconial type at an affordable cost of INR 20,000.

Conclusion

If you or someone you know is experiencing symptoms of CHKB gene muscular dystrophy, congenital, megaconial type, it is important to seek medical advice. A doctor can perform a physical examination and genetic testing to diagnose the condition and provide appropriate treatment. NGS genetic DNA test for CHKB gene muscular dystrophy, congenital, megaconial type is available at DNA Labs India at an affordable cost of INR 20,000.