Blogs

Polycystic Ovary Syndrome (PCOS) is a common condition affecting women of reproductive age, characterized by hormonal imbalance and metabolism problems that can lead to irregular menstrual periods, infertility, and other health issues. The SULT2A1 gene has been identified as one of the genetic markers associated with PCOS, particularly Type 1. Understanding the symptoms of SULT2A1 […]

Polycystic liver disease (PLD) is a rare condition that causes numerous cysts to grow in the liver. These cysts can vary in size and may lead to significant enlargement of the liver over time. Although PLD can occur on its own, it is often found in association with polycystic kidney disease (PKD). One of the […]

Polycystic Kidney Disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The PKD2 gene, specifically, is associated with Type 2 Autosomal Dominant Polycystic Kidney Disease (ADPKD), which is less aggressive but still significantly impacts the kidneys and other organs over time. Recognizing the symptoms of this condition early […]

Polycystic Kidney Disease Type 1 (PKD1) is a severe genetic disorder that affects the kidneys, leading to the development of numerous cysts in these organs. This condition is caused by mutations in the PKHD1 gene and is inherited in an autosomal recessive manner. The disease can lead to various symptoms and complications, significantly impacting an […]

Polycystic Kidney Disease Type 1 (PKD1) is a significant genetic condition that affects the kidneys, leading to the development of numerous cysts. These cysts are noncancerous round sacs containing water-like fluid, which can dramatically enlarge the kidneys while replacing much of their normal structure. This results in a reduction of kidney function and can lead […]

Polycystic Kidney and Hepatic Disease (PKHD1) is a rare, inherited disorder characterized by the development of kidney cysts and liver abnormalities. The PKHD1 gene mutation is the primary cause of this condition, affecting both kidneys’ normal structure and function, and in some cases, leading to significant liver disease. DNA Labs UAE offers a comprehensive genetic […]

The LHX4 gene plays a critical role in the development and functioning of the pituitary gland, which is a vital part of the body’s endocrine system. Mutations in the LHX4 gene can lead to a rare disorder known as Combined Pituitary Hormone Deficiency (CPHD) Type 4. This condition is characterized by a spectrum of symptoms […]

Certainly! Here’s the article structured as requested: Understanding the Symptoms of LHX3 Gene Pituitary Hormone Deficiency Combined Type 3 The LHX3 gene plays a pivotal role in the development and function of the pituitary gland, which is a small but crucial gland located at the base of the brain. This gland is responsible for producing […]

Pigmented Nodular Adrenocortical Disease Type 1, also known as Primary Pigmented Nodular Adrenocortical Disease (PPNAD), is a rare form of adrenal gland disorder that is part of a larger condition known as Carney Complex. It is primarily caused by mutations in the PRKAR1A gene. Understanding the symptoms of this genetic condition is crucial for early […]

Pendred Syndrome is a genetic disorder that affects the inner ear and thyroid gland, leading to hearing loss and a goiter. It is caused by mutations in the SLC26A4 gene, which plays a crucial role in the development and function of these organs. DNA Labs UAE offers a comprehensive genetic test for Pendred Syndrome, aimed […]