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Symptoms and Testing information for ENAM Gene Amelogenesis Imperfecta Type 1C Genetic Test

Amelogenesis Imperfecta (AI) is a hereditary condition that affects the enamel of the teeth, making it thin, improperly formed, or absent altogether. This condition can lead to teeth that are discolored, sensitive, and prone to breakage or loss. Among the various types of AI, Type 1C, linked to mutations in the ENAM gene, presents unique

Symptoms and Testing information for AMELX Gene Amelogenesis Imperfecta Type 1E Genetic Test

Amelogenesis Imperfecta (AI) is a congenital disorder that affects the structure and appearance of the enamel of teeth, leading to dental problems that can significantly impact an individual’s quality of life. Type 1E, associated with mutations in the AMELX gene, is a specific subtype of this condition. DNA Labs UAE offers a comprehensive genetic test

Symptoms and Testing information for AMBN Gene Amelogenesis Imperfecta Type 1F Genetic Test

Amelogenesis Imperfecta (AI) is a genetic condition that affects the development of the enamel, the hard, protective outer layer of the teeth. Type 1F, associated with mutations in the AMBN gene, is a specific subtype of this condition. DNA Labs UAE offers a comprehensive genetic test for this condition, providing invaluable information for affected individuals

Symptoms and Testing information for FAM20A Gene Amelogenesis Imperfecta Type 1G Genetic Test

Amelogenesis Imperfecta (AI) is a congenital disorder that affects the enamel formation of teeth, leading to a variety of dental problems such as increased tooth decay, sensitivity, and aesthetic concerns. Type 1G, associated with mutations in the FAM20A gene, is a rare and specific subtype of this condition. Understanding the symptoms and the availability of

Symptoms and Testing information for ITGB6 Gene Amelogenesis Imperfecta Type 1H Genetic Test

Amelogenesis Imperfecta (AI) is a congenital disorder that affects the dental enamel, impairing its structure and appearance. Among the various types of AI, Type 1H, linked to mutations in the ITGB6 gene, presents unique challenges and symptoms for those affected. DNA Labs UAE offers a comprehensive genetic test for ITGB6 Gene Amelogenesis Imperfecta Type 1H,

Symptoms and Testing information for KLK4 Gene Amelogenesis Imperfecta Type 2A1 Genetic Test

Amelogenesis Imperfecta (AI) is a diverse collection of genetic conditions that affect the development of enamel, the hard, outer layer of teeth. Type 2A1, associated with mutations in the KLK4 gene, is one of the subtypes of this condition. DNA Labs UAE offers a comprehensive genetic test for those who may be affected by or

Symptoms and Testing information for PEX1 Gene Heimler Syndrome Type 1 Genetic Test

Symptoms of PEX1 Gene Heimler Syndrome Type 1 Genetic Test Heimler Syndrome is a rare genetic disorder that is passed down through families in an autosomal recessive pattern. It is primarily characterized by sensorineural hearing loss, dental anomalies, nail abnormalities, and occasionally, visual impairment due to retinal dystrophy. The condition is linked to mutations in

Symptoms and Testing information for MYH14 Gene Deafness Autosomal Dominant Type 4 Genetic Test

Understanding the genetic underpinnings of various conditions can empower individuals with knowledge and options for managing their health. Among these genetic conditions, MYH14 gene-related deafness, known as Autosomal Dominant Type 4, stands out due to its specific inheritance pattern and implications for affected families. This article delves into the symptoms associated with this condition and

Symptoms and Testing information for CYP27B1 Gene Rickets Vitamin D Dependent Type 1 Genetic Test

Symptoms of CYP27B1 Gene Rickets Vitamin D Dependent Type 1 Genetic Test Rickets is a condition that leads to softening and weakening of bones in children due to prolonged vitamin D deficiency. Among its various forms, Vitamin D-dependent rickets type 1 (VDDR-I) is a rare genetic disorder caused by mutations in the CYP27B1 gene. This

Symptoms and Testing information for BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test

Maple Syrup Urine Disease (MSUD) is a rare but serious inherited condition that affects the body’s ability to process certain amino acids, leading to a buildup of these substances in the body. This condition gets its name from the distinctive sweet odor of affected infants’ urine, reminiscent of maple syrup. The BCKDHA gene is crucial

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