Search Results for: feed

Symptoms and Testing information for CTSD Gene Ceroid lipofuscinosis neuronal type 10 Genetic Test

Ceroid lipofuscinosis neuronal type 10 (CLN10) is a rare genetic disorder that is part of a group of diseases known as neuronal ceroid lipofuscinoses (NCLs). These disorders affect the nervous system and are characterized by the accumulation of a fatty substance called lipofuscin in the body’s tissues. The CTSD gene, which provides instructions for producing

Symptoms and Testing information for ASL Gene Argininosuccinic aciduria Genetic Test

Argininosuccinic aciduria is a rare but serious inherited disorder that affects the body’s ability to properly process certain proteins. This condition is part of a group of disorders known as urea cycle disorders, which can lead to a buildup of ammonia in the bloodstream. Early diagnosis and treatment are crucial for managing symptoms and preventing

Symptoms and Testing information for DDC Gene Aromatic L-amino acid decarboxylase deficiency AADC Genetic Test

Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare genetic disorder that affects the way signals are passed between cells in the nervous system. This condition is caused by mutations in the DDC gene, which leads to a deficiency in the AADC enzyme. This enzyme is crucial for the synthesis of neurotransmitters such as dopamine

Symptoms and Testing information for GBE1 Gene Andersen Disease Genetic Test

DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide individuals with insights into their genetic makeup. One of the critical tests offered by DNA Labs UAE is the GBE1 Gene Andersen Disease Genetic Test. This test is crucial for diagnosing Andersen Disease, also known as

Symptoms and Testing information for ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency Genetic Test

Symptoms of ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency Acyl-CoA Short-Chain Dehydrogenase Deficiency (ACADSD) is a rare genetic disorder that affects the body’s ability to break down certain fats into energy, particularly during periods of fasting. This condition is caused by mutations in the ACADS gene, which plays a critical role in the metabolism of short-chain

Symptoms and Testing information for ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test

In the realm of genetic diagnostics and personalized medicine, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic testing services designed to enhance patient care and treatment outcomes. Among these, the ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test is a pivotal diagnostic tool for individuals suspected of having ATIC

Symptoms and Testing information for HIBCH Gene 3-Hydroxyisobutryl-CoA Hydrolase Deficiency Genetic Test

Genetic testing has become a cornerstone in the diagnosis and understanding of various genetic disorders. One such condition, which is rare but significant, is the deficiency of 3-Hydroxyisobutryl-CoA Hydrolase, stemming from mutations in the HIBCH gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the HIBCH Gene 3-Hydroxyisobutryl-CoA Hydrolase

Symptoms and Testing information for MCCC1 Gene 3-Methylcrontonyl-CoA Carboxylase 1 Deficiency Genetic Test

At DNA Labs UAE, we understand the importance of early detection and accurate diagnosis for managing and treating genetic conditions. One such condition is the deficiency of the MCCC1 gene, which encodes the enzyme 3-Methylcrontonyl-CoA Carboxylase 1. This enzyme plays a crucial role in the breakdown of certain proteins and fats in the body. A

Symptoms and Testing information for MCCC2 Gene 3-Methylcrontonyl-CoA Carboxylase 2 Deficiency Genetic Test

At DNA Labs UAE, we are committed to providing comprehensive genetic testing services to help individuals and families understand their genetic health. One of the specialized tests we offer is for the MCCC2 gene, which is crucial for diagnosing 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency. This rare genetic disorder can lead to various health issues if not

Symptoms and Testing information for AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test

3-Methylglutaconic aciduria type 1 is a rare genetic disorder that can lead to various health issues ranging from developmental delays to metabolic abnormalities. This condition is caused by mutations in the AUH gene, which plays a critical role in the body’s leucine metabolism. Understanding the symptoms of this genetic disorder is crucial for early diagnosis