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Symptoms and Testing information for AR Gene Hypospadias Type 1 X-Linked Genetic Test

Symptoms and Testing information for AR Gene Hypospadias Type 1 X-Linked Genetic Test

Hypospadias is a congenital condition marked by an abnormal placement of the urethral opening on the penis. In some cases, this condition is linked to genetic factors, one of which involves mutations in the AR gene. Understanding the implications of these mutations and identifying them early can be crucial for effective management and treatment. The […]

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

Understanding the nuances of genetic disorders is critical for early diagnosis and treatment. Among these disorders, Hypogonadotropic Hypogonadism Type 6, caused by mutations in the FGF8 gene, stands out due to its unique symptoms and implications. This condition can occur with or without anosmia, adding complexity to its diagnosis and management. Recognizing the symptoms early […]

Symptoms and Testing information for DCAF17 Gene Hypogonadism Alopecia Diabetes Mellitus Mental Retardation and Extrapyramidal Syndrome Genetic Test

Symptoms and Testing information for DCAF17 Gene Hypogonadism Alopecia Diabetes Mellitus Mental Retardation and Extrapyramidal Syndrome Genetic Test

In the realm of genetic diagnostics, understanding the intricate web of genes and their potential mutations is crucial for the early detection and management of various inherited conditions. Among these, the DCAF17 gene mutation presents a particularly challenging spectrum of symptoms that necessitates comprehensive genetic testing. DNA Labs UAE stands at the forefront of this […]

Symptoms and Testing information for PIGW Gene Hyperphosphatasia with Mental Retardation Syndrome Type 5 Genetic Test

Symptoms and Testing information for PIGW Gene Hyperphosphatasia with Mental Retardation Syndrome Type 5 Genetic Test

Understanding the genetic underpinnings of various syndromes is crucial in the field of medical genetics. One such condition, Hyperphosphatasia with Mental Retardation Syndrome Type 5 (HPMRS5), also known as Mabry Syndrome, has garnered attention due to its significant impact on affected individuals. This condition is caused by mutations in the PIGW gene, which plays a […]

Symptoms and Testing information for PGAP3 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 4 Genetic Test

Symptoms and Testing information for PGAP3 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 4 Genetic Test

— Hyperphosphatasia with mental retardation syndrome type 4 (HPMRS4), also known as PGAP3 deficiency, is a rare genetic condition that affects various parts of the body, including the brain. This disorder is part of a group of diseases known as glycosylphosphatidylinositol (GPI) biosynthesis defects, which are characterized by intellectual disability, seizures, and skeletal abnormalities due […]

Symptoms and Testing information for PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test

Symptoms and Testing information for PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test

### Article Content: Hyperphosphatasia with Mental Retardation Syndrome Type 3 (HPMRS3), also known as Mabry Syndrome, is a rare genetic disorder characterized by elevated levels of alkaline phosphatase in the blood, intellectual disability, and distinct facial features. This condition is caused by mutations in the PGAP2 gene. Understanding the symptoms and opting for a genetic […]

Symptoms and Testing information for PIGO Gene Hyperphosphatasia with Mental Retardation Syndrome Type 2 Genetic Test

Symptoms and Testing information for PIGO Gene Hyperphosphatasia with Mental Retardation Syndrome Type 2 Genetic Test

— Hyperphosphatasia with mental retardation syndrome (HPMRS), also known as Mabry syndrome, is a rare genetic condition characterized by elevated levels of alkaline phosphatase, intellectual disability, and distinct facial features. One of the genes associated with this condition is the PIGO gene, which plays a critical role in glycosylphosphatidylinositol (GPI) anchor biosynthesis. The GPI anchor […]

Symptoms and Testing information for PIGV Gene Hyperphosphatasia with Mental Retardation Syndrome Type 1 Genetic Test

Symptoms and Testing information for PIGV Gene Hyperphosphatasia with Mental Retardation Syndrome Type 1 Genetic Test

Symptoms of PIGV Gene Hyperphosphatasia with Mental Retardation Syndrome Type 1 Hyperphosphatasia with mental retardation syndrome type 1 (HPMRS1), also known as Mabry syndrome, is a rare genetic disorder caused by mutations in the PIGV gene. This condition is characterized by elevated levels of alkaline phosphatase in the blood, intellectual disability, and various physical anomalies. […]

Symptoms and Testing information for AHCY Gene Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase Genetic Test

Symptoms and Testing information for AHCY Gene Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase Genetic Test

Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase (AHCY) is a rare genetic disorder affecting the body’s ability to process certain amino acids properly. This condition can lead to a range of symptoms and health issues, making it crucial for individuals to understand the potential signs and the importance of genetic testing. DNA Labs UAE offers a […]

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