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Symptoms and Testing information for GNAI3 Gene Auriculocondylar Syndrome Type 1 Genetic Test

Auriculocondylar syndrome (ACS) represents a rare genetic condition, with Auriculocondylar Syndrome Type 1 being one of its forms, primarily resulting from mutations in the GNAI3 gene. This syndrome is characterized by a range of physical malformations that primarily affect the structure of the patient’s face. DNA Labs UAE offers a comprehensive genetic test for those

Symptoms and Testing information for PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test

Auriculocondylar Syndrome Type 2 (ACS2) is a rare genetic disorder that affects the development of the ear, mandible (jawbone), and in some cases, the heart. This condition is primarily caused by mutations in the PLCB4 gene, which plays a crucial role in the development of these structures. Recognizing the symptoms of ACS2 is vital for

Symptoms and Testing information for ASXL3 Gene Bainbridge-Ropers Syndrome Genetic Test

— Bainbridge-Ropers Syndrome (BRS) is a rare genetic disorder that affects multiple aspects of a patient’s health and development. It is caused by mutations in the ASXL3 gene, which plays a crucial role in the regulation of gene expression. DNA Labs UAE offers a comprehensive genetic test for those who suspect they or their family

Symptoms and Testing information for ASXL1 Gene Bohring-Opitz Syndrome Genetic Test

Bohring-Opitz Syndrome (BOS) is a rare genetic disorder that is primarily characterized by severe developmental delays, distinctive facial features, and various physical abnormalities. The syndrome is caused by mutations in the ASXL1 gene, which plays a crucial role in the regulation of gene expression. Recognizing the symptoms of Bohring-Opitz Syndrome is essential for early diagnosis

Symptoms and Testing information for HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome Genetic Test

HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome is a rare genetic condition that has captured the attention of medical researchers and healthcare professionals worldwide. This condition, which stems from mutations in the HOXA1 gene, affects the development of the brainstem and cranial nerves, leading to a range of developmental and neurological challenges. DNA Labs UAE is

Symptoms and Testing information for CRELD1 Gene Atrioventricular Septal Defect Partial with Heterotaxy Syndrome Genetic Test

Understanding the complexities of genetic conditions is essential for early diagnosis and management. One such condition that has garnered attention is the CRELD1 gene-related atrioventricular septal defect partial with heterotaxy syndrome. This condition is a congenital heart defect that is often diagnosed in infancy or early childhood. In this article, we will delve into the

Symptoms and Testing information for HBG2 Gene Cyanosis Transient Neonatal Genetic Test

The HBG2 gene plays a crucial role in the development and functioning of hemoglobin in humans. Mutations in this gene can lead to various blood-related disorders, including transient neonatal cyanosis. This condition is characterized by a blue or purple coloration of the skin, often apparent shortly after birth, indicating that the baby’s blood is not

Symptoms and Testing information for ATRX Gene Alpha-thalassemiamental retardation syndrome Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide individuals with crucial information about their genetic health. Among these, the ATRX Gene Alpha-thalassemia/mental retardation syndrome (ATRX) genetic test stands out for its importance in diagnosing a rare and complex condition. This article delves

Symptoms and Testing information for GATA4 Gene Testicular anomalies with or without congenital heart disease Genetic Test

Understanding the implications and symptoms of GATA4 gene testicular anomalies, with or without congenital heart disease, is crucial for early diagnosis and treatment. This genetic condition, although rare, can have significant impacts on an individual’s health and development. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the GATA4 gene

Symptoms and Testing information for FOXF2 Gene Disorders of sex development with cleft palate Genetic Test

DNA Labs UAE stands at the forefront of genetic testing, offering a wide range of services aimed at providing individuals with the information they need to make informed health and lifestyle decisions. One of the specialized tests offered is focused on the FOXF2 gene, known to be associated with disorders of sex development (DSD) and

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