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Symptoms and Testing information for MFSD8 Gene Ceroid lipofuscinosis neuronal type 7 Genetic Test

Symptoms and Testing information for MFSD8 Gene Ceroid lipofuscinosis neuronal type 7 Genetic Test

Understanding the symptoms associated with MFSD8 gene mutations is crucial for early detection and management of Ceroid Lipofuscinosis Neuronal type 7 (CLN7), a rare but severe neurodegenerative disorder. DNA Labs UAE offers comprehensive genetic testing for CLN7, providing invaluable insights for affected families. This article delves into the symptoms indicative of CLN7, emphasizing the importance […]

Symptoms and Testing information for CLN6 Gene Ceroid lipofuscinosis neuronal type 6 Genetic Test

Symptoms and Testing information for CLN6 Gene Ceroid lipofuscinosis neuronal type 6 Genetic Test

Understanding the symptoms of CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 is crucial for early diagnosis and management of this rare genetic disorder. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including the CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 Genetic Test, to help identify this condition in affected individuals. […]

Symptoms and Testing information for CLN3 Gene Ceroid lipofuscinosis neuronal type 3 Genetic Test

Symptoms and Testing information for CLN3 Gene Ceroid lipofuscinosis neuronal type 3 Genetic Test

Ceroid lipofuscinosis neuronal type 3, commonly known as CLN3 disease or Batten disease, is a rare, inherited, neurodegenerative disorder that primarily affects the nervous system. Early symptoms typically begin in childhood, and the condition progressively leads to a severe decline in motor functions, vision, and mental capabilities. Given the severe impact of CLN3 disease, early […]

Symptoms and Testing information for TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test

Symptoms and Testing information for TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test

Ceroid lipofuscinosis neuronal type 2 (CLN2), also known as tripeptidyl peptidase 1 (TPP1) deficiency, is a rare, genetic, and fatal disorder that affects the nervous system. Children with CLN2 disease experience progressive deterioration of motor skills, speech, vision, and cognitive abilities due to the accumulation of lipopigments in the body’s tissues. These lipopigments, primarily ceroid […]

Symptoms and Testing information for GRN Gene Ceroid lipofuscinosis neuronal type 11 Genetic Test

Symptoms and Testing information for GRN Gene Ceroid lipofuscinosis neuronal type 11 Genetic Test

Understanding the symptoms of GRN Gene Ceroid Lipofuscinosis Neuronal Type 11 (CLN11) is crucial for early diagnosis and management of the condition. This genetic disorder, although rare, has significant impacts on those affected and their families. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including the GRN Gene Ceroid Lipofuscinosis […]

Symptoms and Testing information for PPT1 Gene Ceroid lipofuscinosis neuronal type 1 Genetic Test

Symptoms and Testing information for PPT1 Gene Ceroid lipofuscinosis neuronal type 1 Genetic Test

Symptoms of PPT1 Gene Ceroid Lipofuscinosis Neuronal Type 1 Genetic Test Ceroid lipofuscinosis neuronal type 1 (CLN1), also known as infantile Batten disease, is a rare and fatal autosomal recessive neurodegenerative disorder that primarily affects the nervous system. It is caused by mutations in the PPT1 gene, which leads to the accumulation of lipopigments in […]

Symptoms and Testing information for COMT Gene Catechol-o-methyltransferase deficiency Genetic Test

Symptoms and Testing information for COMT Gene Catechol-o-methyltransferase deficiency Genetic Test

The COMT (Catechol-O-Methyltransferase) gene plays a critical role in the metabolic process of catecholamines, such as dopamine, epinephrine, and norepinephrine. These neurotransmitters are essential for various bodily functions, including mood regulation, cognition, and response to stress. A deficiency in the COMT enzyme can lead to a variety of symptoms and conditions, making it crucial for […]

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