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Symptoms and Testing information for SDHC Gene Pheochromocytoma Type 3 Genetic Test

Symptoms and Testing information for SDHC Gene Pheochromocytoma Type 3 Genetic Test

Symptoms of SDHC Gene Pheochromocytoma Type 3 Genetic Test Pheochromocytoma is a rare tumor of the adrenal gland tissue. It results in the gland producing an excess amount of adrenaline. Pheochromocytoma can occur at any age, but it most commonly affects people between the ages of 20 and 50. Type 3 Pheochromocytoma, associated with mutations […]

Symptoms and Testing information for SDHB Gene Pheochromocytoma Type 2 Genetic Test

Symptoms and Testing information for SDHB Gene Pheochromocytoma Type 2 Genetic Test

In the realm of genetic testing and personalized medicine, understanding the intricacies of our genetic makeup has never been more critical. Among the various genetic tests available, the SDHB Gene Pheochromocytoma Type 2 Genetic Test stands out for its significance in diagnosing a rare but potentially severe condition. This test, offered by DNA Labs UAE, […]

Symptoms and Testing information for SDHD Gene Pheochromocytoma Type 1 Genetic Test

Symptoms and Testing information for SDHD Gene Pheochromocytoma Type 1 Genetic Test

Pheochromocytoma is a rare tumor of the adrenal gland tissue, which results in the excessive production of adrenaline and noradrenaline, hormones that regulate heart rate, metabolism, and blood pressure. SDHD gene mutations are linked to a predisposition to develop this type of tumor, classified under Pheochromocytoma Type 1. DNA Labs UAE offers a comprehensive genetic […]

Symptoms and Testing information for STK11 Gene Peutz-Jeghers Syndrome Genetic Test

Symptoms and Testing information for STK11 Gene Peutz-Jeghers Syndrome Genetic Test

Symptoms of STK11 Gene Peutz-Jeghers Syndrome Peutz-Jeghers Syndrome (PJS) is a genetic condition characterized by the development of benign polyps in the gastrointestinal tract and distinctive pigmented spots on the skin. It is caused by mutations in the STK11 gene, which plays a critical role in regulating cell growth and division. Individuals with PJS are […]

Symptoms and Testing information for SDHA Gene Paragangliomas Type 5 Genetic Test

Symptoms and Testing information for SDHA Gene Paragangliomas Type 5 Genetic Test

In the realm of genetic diagnostics and personalized medicine, the identification of specific gene mutations that can lead to certain diseases has become a cornerstone of preventive healthcare. One such condition, Paragangliomas Type 5, is associated with mutations in the SDHA gene. This condition, though rare, necessitates a deeper understanding and awareness, particularly regarding its […]

Symptoms and Testing information for SDHB Gene Paragangliomas Type 4 Genetic Test

Symptoms and Testing information for SDHB Gene Paragangliomas Type 4 Genetic Test

Paragangliomas are rare neuroendocrine tumors that can develop at various body sites, including the head, neck, thorax, and abdomen. Type 4 Paragangliomas are specifically associated with mutations in the SDHB (succinate dehydrogenase complex, subunit B) gene. These tumors can be either benign or malignant and may produce excessive amounts of catecholamines, which are hormones that […]

Symptoms and Testing information for SDHD Gene Paraganglioma and Gastric Stromal Sarcoma Genetic Test

Symptoms and Testing information for SDHD Gene Paraganglioma and Gastric Stromal Sarcoma Genetic Test

Understanding the complexities of genetic conditions is crucial for early diagnosis and treatment. Among these, SDHD gene paraganglioma and gastric stromal sarcoma stand out due to their significant impact on individuals’ health. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the SDHD Gene Paraganglioma and Gastric Stromal Sarcoma Genetic […]

Symptoms and Testing information for CDKN2A Gene Pancreatic Cancer-Melanoma Syndrome Familial Genetic Test

Symptoms and Testing information for CDKN2A Gene Pancreatic Cancer-Melanoma Syndrome Familial Genetic Test

Pancreatic cancer-melanoma syndrome, also known as familial atypical multiple mole melanoma (FAMMM) syndrome, is a condition characterized by an increased risk of developing melanoma and pancreatic cancer. This syndrome is primarily associated with mutations in the CDKN2A gene. Understanding the symptoms and genetic predispositions of this syndrome is crucial for early detection and management. DNA […]

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