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Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, which are tiny, hair-like structures that line the airways, reproductive system, and other parts of the body. These cilia play a crucial role in moving mucus and other materials out of the airways, ensuring the proper functioning of the respiratory system, and facilitating movement of sperm and egg in the reproductive system. One of the genes associated with this condition is the RSPH4A gene, and mutations in this gene can lead to Primary Ciliary Dyskinesia Type 11.
Symptoms of RSPH4A Gene Primary Ciliary Dyskinesia Type 11 can vary widely among individuals but typically include chronic respiratory tract infections, which can lead to a condition known as bronchiectasis, where the airways are permanently widened and scarred. Other common symptoms include:
– Chronic wet cough
– Recurrent ear infections, which may lead to hearing loss
– Sinusitis
– Situs inversus (where internal organs are mirrored from their normal positions)
– Infertility issues due to impaired sperm motility or dysfunctional movement of the fallopian tubes
Early diagnosis and treatment are crucial in managing the symptoms and improving the quality of life for those affected by this condition. DNA Labs UAE offers a genetic test for the RSPH4A Gene Primary Ciliary Dyskinesia Type 11, which can help in the early detection and management of this condition. The test cost is 4400 AED.
For more information on the RSPH4A Gene Primary Ciliary Dyskinesia Type 11 Genetic Test, visit [DNA Labs UAE](https://dnalabsuae.com/tests/rsph4a-gene-primary-ciliary-dyskinesia-type-11-genetic-test/).
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Symptoms of RSPH4A Gene Primary Ciliary Dyskinesia Type 11
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, which are tiny, hair-like structures that line the airways, reproductive system, and other parts of the body. These cilia play a crucial role in moving mucus and other materials out of the airways, ensuring the proper functioning of the respiratory system, and facilitating movement of sperm and egg in the reproductive system. One of the genes associated with this condition is the RSPH4A gene, and mutations in this gene can lead to Primary Ciliary Dyskinesia Type 11.
Symptoms of RSPH4A Gene Primary Ciliary Dyskinesia Type 11 can vary widely among individuals but typically include chronic respiratory tract infections, which can lead to a condition known as bronchiectasis, where the airways are permanently widened and scarred. Other common symptoms include:
- Chronic wet cough
- Recurrent ear infections, which may lead to hearing loss
- Sinusitis
- Situs inversus (where internal organs are mirrored from their normal positions)
- Infertility issues due to impaired sperm motility or dysfunctional movement of the fallopian tubes
Early diagnosis and treatment are crucial in managing the symptoms and improving the quality of life for those affected by this condition. DNA Labs UAE offers a genetic test for the RSPH4A Gene Primary Ciliary Dyskinesia Type 11, which can help in the early detection and management of this condition. The test cost is 4400 AED.
For more information on the RSPH4A Gene Primary Ciliary Dyskinesia Type 11 Genetic Test, visit DNA Labs UAE.
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