Metabolic Disorders

Symptoms of AVPR2 Gene Diabetes Insipidus Nephrogenic X-Linked Genetic Test Diabetes insipidus (DI) is a rare condition that occurs when your kidneys are unable to conserve water. Nephrogenic diabetes insipidus (NDI) is a distinct form of the disease that is caused by the kidneys’ insensitivity to the antidiuretic hormone vasopressin. This insensitivity can be due […]

In the realm of medical genetics, the understanding and diagnosis of rare conditions have significantly advanced with the advent of comprehensive genetic testing. One such condition that has garnered attention for its precise diagnosis through genetic testing is Neurohypophyseal Diabetes Insipidus, particularly the type influenced by mutations in the AVP gene. DNA Labs UAE stands […]

Diabetes mellitus type 1, also known as type 1 diabetes, is a form of diabetes mellitus that results from the autoimmune destruction of the insulin-producing beta cells in the pancreas. The subsequent lack of insulin leads to increased blood and urine glucose. The classical symptoms are frequent urination, increased thirst, increased hunger, and weight loss. […]

In the realm of genetic testing and diagnosis, understanding the nuances of specific conditions is crucial for both patients and healthcare providers. Among these conditions, diabetes mellitus insulin-dependent type 20, linked to mutations in the HNF1A gene, represents a significant area of interest due to its unique characteristics and implications for treatment. DNA Labs UAE […]

Symptoms of INSR Gene Diabetes Mellitus Insulin-Resistant with Acanthosis Nigricans Genetic Test Diabetes Mellitus, particularly the insulin-resistant type with Acanthosis Nigricans, is a complex and challenging condition that affects a significant number of individuals globally. This condition is primarily associated with mutations in the INSR gene, which plays a crucial role in the body’s insulin […]

Symptoms of GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test Diabetes mellitus neonatal, a rare form of diabetes, is primarily caused by genetic mutations, one of which is found in the GLIS3 gene. This condition manifests early in life, often immediately after birth or within the first six months. Recognizing the symptoms early is crucial for […]

Diabetes mellitus is a chronic condition that affects millions of people worldwide. Among its various types, noninsulin-dependent diabetes mellitus (NIDDM), also known as Type 2 diabetes, is the most common. Recent advancements in genetic research have uncovered that mutations in the ABCC8 gene can significantly influence the development of this type of diabetes. Understanding the […]

In recent years, the medical field has witnessed remarkable advancements in understanding and diagnosing various genetic conditions. Among these developments, the role of genetic testing has become increasingly significant, particularly in the diagnosis and management of diabetes mellitus. One such breakthrough is the identification of the AKT2 gene’s involvement in noninsulin-dependent diabetes mellitus, also known […]

Diabetes mellitus, a condition characterized by high blood sugar levels over a prolonged period, is a global health concern. Among the types of diabetes, noninsulin-dependent diabetes mellitus (NIDDM), also known as Type 2 diabetes, is the most common. Recent advancements in genetic research have unveiled the role of specific genes in the development of NIDDM, […]

Cystic fibrosis is a complex genetic disorder that affects the lungs and digestive system. It is caused by mutations in the CFTR gene, which are well-known. However, recent research has indicated that mutations in other genes, such as SLC6A14, can also contribute to the severity and manifestations of cystic fibrosis. Understanding the role of the […]