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Symptoms and Testing information for BMP4 Gene Orofacial Cleft Type 11 Genetic Test

Orofacial clefts are among the most common congenital anomalies, affecting numerous infants worldwide each year. These conditions can significantly impact an individual’s quality of life, affecting their ability to eat, speak, hear, and breathe properly. Advances in genetic testing have paved the way for early detection and intervention, offering hope to many families. Among these

Symptoms and Testing information for MSX1 Gene Orofacial Cleft Type 5 Genetic Test

Orofacial clefts, comprising cleft lip and cleft palate anomalies, are among the most common congenital malformations, affecting approximately 1 in every 700 live births globally. These conditions not only impact the physical appearance but can also lead to significant functional challenges, including difficulties with feeding, speech, hearing, and dental development. Recent advancements in genetics have

Symptoms and Testing information for NECTIN1 Gene Orofacial Cleft Type 7 Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide individuals with valuable insights into their genetic makeup. Among the various tests offered, the NECTIN1 Gene Orofacial Cleft Type 7 Genetic Test is a crucial diagnostic tool for families and individuals concerned about the

Symptoms and Testing information for DDX59 Gene Orofaciodigital Syndrome Type 5 Genetic Test

Symptoms of DDX59 Gene Orofaciodigital Syndrome Type 5 Genetic Test Orofaciodigital Syndrome Type 5 (OFD5), a rare genetic disorder, is marked by a distinctive pattern of physical features and abnormalities that affect the oral cavity, facial features, and digits. This condition is linked to mutations in the DDX59 gene, and understanding its symptoms is crucial

Symptoms and Testing information for STAC3 Gene Native American Myopathy Genetic Test

Native American Myopathy (NAM) is a rare genetic disorder that predominantly affects individuals of Native American descent, although it can occur in other populations. It is caused by mutations in the STAC3 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for

Symptoms and Testing information for MED12 Gene Opitz-Kaveggia Syndrome Genetic Test

Symptoms of MED12 Gene Opitz-Kaveggia Syndrome Genetic Test The MED12 gene plays a crucial role in the development of the nervous system and other bodily functions. Mutations in the MED12 gene can lead to a rare condition known as Opitz-Kaveggia Syndrome. This condition, also known as FG syndrome, affects many parts of the body and

Symptoms and Testing information for SUMO1 Gene Orofacial Cleft Type 10 Genetic Test

In the realm of genetic diagnostics and personalized medicine, understanding the intricate details of our genetic makeup has become increasingly vital. One such area of focus is the study of the SUMO1 gene and its link to orofacial cleft type 10. At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the

Symptoms and Testing information for CENPJ Gene Microcephaly Autosomal Recessive Type 6 Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services aimed at providing precise, actionable insights into your genetic health. One of the critical tests provided by DNA Labs UAE is the CENPJ Gene Microcephaly Autosomal Recessive Type 6 Genetic Test. This test is crucial for families

Symptoms and Testing information for CEP63 Gene Microcephaly CEP63 Related Genetic Test

Microcephaly is a medical condition characterized by a smaller than average head size, which often leads to developmental delays and neurological problems in affected individuals. This condition can be caused by a variety of factors, including infections during pregnancy, exposure to toxic substances, and genetic abnormalities. Among the genetic causes of microcephaly, mutations in the

Symptoms and Testing information for YWHAE Gene Miller Dieker Lissencephaly Syndrome Genetic Test

Symptoms of YWHAE Gene Miller Dieker Lissencephaly Syndrome Genetic Test Miller-Dieker Lissencephaly Syndrome (MDLS) is a rare genetic disorder characterized by a smooth brain surface and a reduction in the number of brain folds and grooves. This condition is associated with mutations in the YWHAE gene, among others, and leads to significant neurological and developmental