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Symptoms and Testing information for COL11A1 Gene Marshall Syndrome Genetic Test

Symptoms of COL11A1 Gene Marshall Syndrome Genetic Test Marshall Syndrome, a genetic disorder caused by mutations in the COL11A1 gene, presents a variety of symptoms that can significantly impact an individual’s quality of life. Recognizing these symptoms early can lead to timely intervention and management. DNA Labs UAE offers a comprehensive genetic test for Marshall

Symptoms and Testing information for MSRB3 Gene Deafness Autosomal Recessive Type 74 Genetic Test

In the realm of genetic testing and diagnostics, the MSRB3 gene deafness autosomal recessive type 74 (DFNB74) represents a significant area of focus for those looking to understand the genetic basis of certain types of hearing loss. At DNA Labs UAE, we offer a comprehensive genetic test designed to identify mutations in the MSRB3 gene,

Symptoms and Testing information for COG7 Gene Glycosylation Disorder Type 2E Genetic Test

— Understanding the symptoms of COG7 Gene Glycosylation Disorder Type 2E is crucial for early diagnosis and management of this rare condition. At DNA Labs UAE, we offer a comprehensive genetic test specifically designed to identify mutations in the COG7 gene, which is pivotal in diagnosing this disorder. The cost of the test is 4400

Symptoms and Testing information for CYP2B6 Gene Efavirenz poor metabolism of Genetic Test

Symptoms of CYP2B6 Gene Efavirenz Poor Metabolism of Genetic Test The CYP2B6 gene plays a pivotal role in the metabolism of various substances within the body, including the antiretroviral medication, Efavirenz, which is commonly used in the treatment of HIV. Variations in the CYP2B6 gene can lead to poor metabolism of Efavirenz, resulting in higher

Symptoms and Testing information for FANCF Gene Fanconi anemia type F Genetic Test

Symptoms of FANCF Gene Fanconi Anemia Type F Genetic Test Fanconi Anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. It is caused by genetic mutations in one of several genes, with the FANCF gene being one such example. This condition is characterized by physical abnormalities, bone marrow failure, and

Symptoms and Testing information for CYP2C9 Gene CoumarinWarfarin resistance due to CYP2C9 variants Genetic Test

In the realm of personalized medicine, understanding the genetic makeup of an individual has become paramount, especially in the context of drug metabolism. One such area of focus is the impact of genetic variations on the metabolism of Coumarin/Warfarin, a commonly prescribed anticoagulant. The CYP2C9 gene plays a crucial role in this process, and variants

Symptoms and Testing information for ABCB1 Gene Colchicine resistance Genetic Test

Understanding the ABCB1 Gene and Its Implications on Colchicine Resistance Colchicine is a medication commonly used in the treatment of gout and certain other medical conditions. However, not all patients respond to colchicine treatment effectively. This variability in response can often be attributed to genetic factors, particularly the ABCB1 gene. The ABCB1 gene encodes for

Symptoms and Testing information for HGD Gene Alkaptonuria Genetic Test

Alkaptonuria, a rare genetic disorder, affects one in every 250,000 to 1 million individuals worldwide. This condition arises due to a deficiency in the enzyme homogentisate 1,2-dioxygenase (HGD), which is crucial for breaking down the amino acids tyrosine and phenylalanine. The lack of this enzyme’s activity leads to the accumulation of homogentisic acid in the

Symptoms and Testing information for KCNC3 Gene Spinocerebellar Ataxia Type 13 Autosomal Dominant Genetic Test

DNA Labs UAE is at the forefront of genetic testing and analysis, offering a comprehensive range of services designed to provide individuals with insights into their genetic makeup. Among the various tests available, the KCNC3 Gene Spinocerebellar Ataxia Type 13 Autosomal Dominant Genetic Test is a critical tool for individuals and families concerned about the

Symptoms and Testing information for AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test

Symptoms of AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test Spinal and Bulbar Muscular Atrophy (SBMA), also known as Kennedy’s Disease, is a rare, X-linked recessive genetic disorder that primarily affects males. It is caused by mutations in the androgen receptor (AR) gene, leading to the degeneration of motor neurons in the spinal

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