Short Description

NGS genetic DNA test detecets for variant and mutation detection in THRA gene for Hypothyroidism congenital nongoitrous type 6

PreTest Information

Clinical History of Patient who is going for THRA Gene Hypothyroidism congenital nongoitrous type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with THRA Gene Hypothyroidism congenital nongoitrous type 6 NGS Genetic DNA Test gene THRA

Detail Description

THRA Gene Hypothyroidism Congenital Nongoitrous Type 6 NGS Genetic DNA Test: Symptoms, Diagnosis, and Cost

Hypothyroidism is a condition in which the thyroid gland does not produce enough thyroid hormones. This can lead to a variety of symptoms, including fatigue, weight gain, and depression. Congenital nongoitrous hypothyroidism is a rare form of the condition that is present at birth. The THRA gene is one of the genes associated with this type of hypothyroidism.

Symptoms of THRA Gene Hypothyroidism Congenital Nongoitrous Type 6

The symptoms of THRA gene hypothyroidism congenital nongoitrous type 6 can vary from person to person, but may include:

• Jaundice (yellowing of the skin and eyes)
• Poor feeding and slow growth
• Constipation
• Low body temperature
• Delayed development of motor skills
• Developmental delay
• Enlarged thyroid gland (goiter)
• Intellectual disability

Diagnosis of THRA Gene Hypothyroidism Congenital Nongoitrous Type 6

Diagnosis of THRA gene hypothyroidism congenital nongoitrous type 6 is typically made through a blood test that measures the levels of thyroid hormones and thyroid-stimulating hormone (TSH) in the body. If the levels of thyroid hormones are low and the levels of TSH are high, it may indicate hypothyroidism. Genetic testing can also be used to identify mutations in the THRA gene that are associated with this type of hypothyroidism.

NGS Genetic DNA Test for THRA Gene Hypothyroidism Congenital Nongoitrous Type 6

Next-generation sequencing (NGS) genetic DNA testing can be used to detect mutations in the THRA gene that are associated with congenital nongoitrous hypothyroidism. This type of testing can be done using a blood or saliva sample and can detect mutations in multiple genes at once. The cost of NGS genetic DNA testing for THRA gene hypothyroidism congenital nongoitrous type 6 in India is approximately INR 20,000.

Conclusion

THRA gene hypothyroidism congenital nongoitrous type 6 is a rare form of hypothyroidism that is present at birth. Symptoms may include jaundice, poor feeding, constipation, low body temperature, delayed development, and intellectual disability. Diagnosis is typically made through a blood test and genetic testing can be used to identify mutations in the THRA gene. NGS genetic DNA testing for THRA gene hypothyroidism congenital nongoitrous type 6 in India costs approximately INR 20,000.

If you or someone you know is experiencing symptoms of hypothyroidism, it is important to speak with a healthcare provider for proper diagnosis and treatment.

For more information on genetic testing and DNA labs in India, visit DNA Labs India.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for THRA Gene Hypothyroidism congenital nongoitrous type 6 NGS Genetic DNA Test