Symptoms and Testing information for HOXA13 Gene Guttmacher syndrome Genetic Test

Symptoms and Testing information for HOXA13 Gene Guttmacher syndrome Genetic Test

Guttmacher syndrome, also known as hand-foot-genital syndrome, is a rare genetic condition that affects the development of the hands, feet, and genitourinary system. This condition is caused by mutations in the HOXA13 gene, which plays a critical role in the embryonic development of these structures. Understanding the symptoms of Guttmacher syndrome is crucial for early […]

Symptoms and Testing information for HOXA13 Gene Hand-foot-uterus syndrome Genetic Test

Symptoms and Testing information for HOXA13 Gene Hand-foot-uterus syndrome Genetic Test

Hand-foot-uterus syndrome, also known as hand-foot-genital syndrome, is a rare genetic condition that affects the development of the hands, feet, and urogenital system. This condition is caused by mutations in the HOXA13 gene, which plays a crucial role in the embryonic development of these structures. Understanding the symptoms and seeking timely genetic testing can be […]

Symptoms and Testing information for NLRP7 Gene Hydatidiform mole Genetic Test

Symptoms and Testing information for NLRP7 Gene Hydatidiform mole Genetic Test

In the quest to understand the complexities of human genetics and its implications on health, DNA Labs UAE stands at the forefront, offering a range of genetic testing services designed to provide insights into various genetic conditions. Among these, the NLRP7 Gene Hydatidiform Mole Genetic Test is particularly significant for its role in diagnosing a […]

Symptoms and Testing information for KHDC3L Gene Hydatidiform mole recurrent type 2 Genetic Test

Symptoms and Testing information for KHDC3L Gene Hydatidiform mole recurrent type 2 Genetic Test

Hydatidiform mole, also known as a molar pregnancy, is a rare condition that occurs during pregnancy. The condition is characterized by the abnormal growth of trophoblasts, the cells that normally develop into the placenta. There are two types of hydatidiform moles: complete and partial. In some cases, women may experience recurrent hydatidiform moles, a condition […]

Symptoms and Testing information for KISS1 Gene Hypogonadotropic hypogonadism Genetic Test

Symptoms and Testing information for KISS1 Gene Hypogonadotropic hypogonadism Genetic Test

Understanding the complexities of our genetic makeup can unlock answers to numerous health conditions that were once shrouded in mystery. One such condition is Hypogonadotropic Hypogonadism (HH), a disorder characterized by the inadequate secretion of gonadotropin-releasing hormone by the hypothalamus, which affects the development and function of the gonads (ovaries or testes). This can lead […]

Symptoms and Testing information for NSMF Gene Hypogonadotropic hypogonadism Genetic Test

Symptoms and Testing information for NSMF Gene Hypogonadotropic hypogonadism Genetic Test

Symptoms of NSMF Gene Hypogonadotropic Hypogonadism Genetic Test Hypogonadotropic hypogonadism (HH) is a condition characterized by the inadequate secretion of sex hormones due to the malfunctioning of the gonadotropin-releasing hormone (GnRH) in the hypothalamus or the pituitary gland’s response to GnRH. When this condition is linked to mutations in the NSMF gene, it is essential […]

Symptoms and Testing information for FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia Genetic Test

Symptoms and Testing information for FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia Genetic Test

Symptoms of FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or Without Anosmia Genetic Test Hypogonadotropic hypogonadism type 6, caused by mutations in the FGF8 gene, is a condition that affects the development and function of the gonads, leading to reduced or absent production of sex hormones and, consequently, delayed or absent puberty. This condition can […]

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