Genetic mapping for gynecological disorders is a cutting-edge approach that is revolutionizing the way healthcare professionals diagnose and treat various conditions affecting women’s reproductive health. This sophisticated testing method delves into an individual’s DNA to identify specific genetic markers associated with a range of gynecological diseases, offering a personalized and precise diagnosis. DNA Labs UAE […]
Reproductive Diseases
Symptoms and Testing information for Abortion Panel Anti-HLA Antibodies Test
In the realm of medical diagnostics and patient care, the advancement of genetic testing has opened new doors to understanding complex health issues. One such area where genetic testing has proven to be invaluable is in the assessment and management of reproductive health, particularly in cases of recurrent spontaneous abortions (RSA). DNA Labs UAE stands […]
Symptoms and Testing information for BMP15 Gene Ovarian dysgenesis type 2 Genetic Test
Ovarian dysgenesis type 2, a rare genetic disorder, is primarily caused by mutations in the BMP15 gene. The BMP15 gene plays a crucial role in the development of female reproductive organs, particularly the ovaries. When mutations occur in this gene, it can lead to significant reproductive challenges, including infertility. Understanding the symptoms associated with this […]
Symptoms and Testing information for NANOS1 Gene Oligo-astheno-teratozoospermia Genetic Test
In the realm of genetic testing and diagnostics, the advancements have been nothing short of revolutionary, particularly in the field of reproductive health. One such advancement is the genetic testing for conditions affecting fertility, including the NANOS1 gene related oligo-astheno-teratozoospermia. DNA Labs UAE stands at the forefront of these innovations, offering comprehensive genetic testing services […]
Symptoms and Testing information for ZP1 Gene Oocyte maturation defect Genetic Test
The ZP1 gene plays a crucial role in the oocyte maturation process, which is essential for successful fertilization and subsequent embryo development. Mutations in the ZP1 gene can lead to oocyte maturation defects, potentially causing infertility in women. Understanding the symptoms associated with ZP1 gene mutations and the availability of genetic testing is crucial for […]
Symptoms and Testing information for SOHLH1 Gene Oogenesis dysfunction Genetic Test
Symptoms of SOHLH1 Gene Oogenesis Dysfunction Genetic Test Oogenesis, the process by which the female gametes, or ova, are produced, is fundamental to fertility and reproductive health. A key gene implicated in this complex process is SOHLH1, which plays a crucial role in the early stages of oogenesis. Dysfunctions in the SOHLH1 gene can lead […]
Symptoms and Testing information for FSHR Gene Ovarian dysgenesis type 1 Genetic Test
Ovarian dysgenesis type 1 is a rare genetic condition that affects the normal development of the ovaries in females. It is primarily caused by mutations in the FSHR gene, which plays a critical role in the reproductive system. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers […]
Symptoms and Testing information for AMH Gene Persistent Mullerian duct syndrome type 1 Genetic Test
Persistent Mullerian Duct Syndrome (PMDS) is a rare genetic condition that affects males. It is characterized by the presence of female reproductive structures such as a uterus and fallopian tubes, which normally should not be present in a male’s anatomy. This condition arises due to mutations in the AMH gene, leading to Type 1 PMDS. […]
Symptoms and Testing information for AMHR2 Gene Persistent Mullerian duct syndrome type 2 Genetic Test
Persistent Mullerian Duct Syndrome (PMDS) is a rare genetic condition that affects males. It is characterized by the persistence of female reproductive structures, such as the uterus and fallopian tubes, in a genetically male body. This condition is caused by mutations in the AMHR2 gene, which plays a crucial role in the regression of the […]
Symptoms and Testing information for CORIN Gene Preeclampsiaeclampsia type 5 Genetic Test
Preeclampsia is a complex condition that affects pregnant women, typically after the 20th week of pregnancy. It is characterized by high blood pressure and often a significant amount of protein in the urine. The CORIN gene plays a crucial role in the cardiovascular system, and mutations in this gene have been linked to an increased […]