Short Description

This assay detects mutations in the mitochondrial DNA which are responsible for maternal inheritance of Cardiomyopathies.

PreTest Information

Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Detail Description

MICM (Maternally Inherited Cardiomyopathy) Mutation Detection Test: Symptoms, Diagnosis, and Cost

MICM or Maternally Inherited Cardiomyopathy is a genetic disorder that affects the heart muscles. It is a rare condition that is inherited from the mother's side. The condition is caused by a mutation in the mitochondrial DNA that is responsible for providing energy to the cells. The mutation affects the heart muscles, leading to weakened heart muscles and, in severe cases, heart failure.

Symptoms of MICM

The symptoms of MICM are similar to other types of cardiomyopathy. The symptoms include:

• Shortness of breath
• Chest pain
• Fatigue
• Dizziness
• Swelling in the legs, ankles, and feet

The symptoms of MICM usually appear in adolescence or early adulthood. However, some people may not show any symptoms until later in life.

Diagnosis of MICM

MICM is diagnosed using several tests, including:

• Electrocardiogram (ECG)
• Echocardiogram
• Magnetic resonance imaging (MRI)
• Genetic testing

The genetic testing involves analyzing the mitochondrial DNA for mutations that are associated with MICM. The test is usually recommended for people who have a family history of the condition or those who exhibit symptoms of cardiomyopathy.

MICM Mutation Detection Test Cost

The cost of the MICM mutation detection test in India is INR 10500. The test is performed by DNA Labs India, a leading genetic testing laboratory in India. The test involves analyzing the mitochondrial DNA for mutations that are associated with MICM. The test is non-invasive and involves taking a small blood sample from the patient.

The MICM mutation detection test is a highly accurate test that can help in the early detection of the condition. Early detection can help in the timely management of the condition, leading to better outcomes for the patients.

Conclusion

MICM is a rare genetic condition that affects the heart muscles. The condition is inherited from the mother's side and is caused by a mutation in the mitochondrial DNA. The symptoms of MICM are similar to other types of cardiomyopathy and include shortness of breath, chest pain, fatigue, dizziness, and swelling in the legs, ankles, and feet.

The MICM mutation detection test is a highly accurate test that can help in the early detection of the condition. The test is performed by DNA Labs India and costs INR 10500. Early detection of MICM can help in the timely management of the condition, leading to better outcomes for the patients.

This assay detects mutations in the mitochondrial DNA which are responsible for maternal inheritance of Cardiomyopathies.