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Symptoms and Testing information for SUMO1 Gene Orofacial Cleft Type 10 Genetic Test

In the realm of genetic diagnostics and personalized medicine, understanding the intricate details of our genetic makeup has become increasingly vital. One such area of focus is the study of the SUMO1 gene and its link to orofacial cleft type 10. At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the

Symptoms and Testing information for KIF11 Gene Microcephaly with or without Chorioretinopathy Lymphedema or Mental Retardation MCLMR Genetic Test

Symptoms of KIF11 Gene Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation (MCLMR) Genetic Test Understanding the symptoms associated with KIF11 Gene Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation (MCLMR) is crucial for early diagnosis and management of this rare genetic disorder. The KIF11 gene plays a significant role in cell division

Symptoms and Testing information for FGD1 Gene Faciogenital Dysplasia Genetic Test

Faciogenital dysplasia, also known as Aarskog-Scott syndrome, is a rare genetic disorder that primarily affects the development of the face, hands, and genitals. It is caused by mutations in the FGD1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for the

Symptoms and Testing information for FOXH1 Gene Congenital Heart Disease and Transposition of the Great Arteries Genetic Test

Symptoms of FOXH1 Gene Congenital Heart Disease Congenital heart disease (CHD) refers to a range of birth defects that affect the normal workings of the heart. The FOXH1 gene has been identified as one of the genetic factors contributing to the development of congenital heart disease, including the transposition of the great arteries (TGA). TGA

Symptoms and Testing information for GP1BA Gene von Willebrand Disease Platelet Type Genetic Test

In the intricate landscape of genetic disorders, von Willebrand Disease (VWD) stands out due to its impact on blood clotting. Among its types, the Platelet Type von Willebrand Disease (PT-VWD), associated with mutations in the GP1BA gene, presents unique challenges in diagnosis and management. DNA Labs UAE, a leading genetic testing facility, offers a comprehensive

Symptoms and Testing information for TTC21B Gene Nephronophthisis Type 12 Genetic Test

Nephronophthisis (NPHP) is a genetic disorder that primarily affects the kidneys. It is the most common genetic cause of chronic kidney disease in children and young adults. NPHP Type 12, specifically, is caused by mutations in the TTC21B gene. Understanding the symptoms and getting a timely diagnosis can significantly impact the management and outcome of

Symptoms and Testing information for MKKS Gene McKusick-Kaufman Syndrome Genetic Test

Symptoms of MKKS Gene McKusick-Kaufman Syndrome Genetic Test MKKS Gene McKusick-Kaufman Syndrome is a rare genetic disorder that affects multiple organ systems in the body, including the limbs, heart, and the reproductive system. Understanding the symptoms of this syndrome is crucial for early diagnosis and management. The genetic test for MKKS Gene McKusick-Kaufman Syndrome, offered

Symptoms and Testing information for FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Test

Understanding the Symptoms of FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Disorder Interstitial nephritis is a critical condition that affects the kidneys by causing inflammation of the spaces between the kidney tubules. When this condition is linked to the FAN1 gene, it becomes a part of a rare genetic disorder known as Karyomegalic Interstitial Nephritis (KIN).

Symptoms and Testing information for ESR1 Gene Estrogen Resistance Genetic Test

Symptoms of ESR1 Gene Estrogen Resistance Genetic Test The ESR1 gene plays a pivotal role in mediating the effects of estrogen, a crucial hormone in the development and function of both female and male reproductive systems. Mutations in the ESR1 gene can lead to estrogen resistance, a rare condition that can have significant implications on

Symptoms and Testing information for ABCA1 Gene Coronary Artery Disease in Familial Hypercholesterolemia Protection Against Genetic Test

Understanding the intricate relationship between genetics and coronary artery disease is crucial, especially when it comes to familial hypercholesterolemia (FH). This condition, which often goes undiagnosed, puts individuals at a higher risk for early-onset coronary artery disease. However, advancements in genetic testing, particularly concerning the ABCA1 gene, have opened new avenues for identifying and managing

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