Symptoms of AR Gene Spinal and Bulbar Muscular Atrophy X-Linked Genetic Test Spinal and Bulbar Muscular Atrophy (SBMA), also known as Kennedy’s Disease, is a rare, X-linked recessive genetic disorder that primarily affects males. It is caused by mutations in the androgen receptor (AR) gene, leading to the degeneration of motor neurons in the spinal […]
Spinal Muscular Atrophy Distal Autosomal Recessive Type 4 (SMA-DAR4), also known as Spinal Muscular Atrophy with Lower Extremity Predominance 2 (SMA-LED2), is a rare genetic disorder caused by mutations in the PLEKHG5 gene. This condition is characterized by progressive muscle weakness and atrophy, predominantly affecting the lower limbs. The disease’s onset can vary from early […]
Symptoms of NIPA1 Gene SPG6 Genetic Test The NIPA1 gene is associated with a condition known as Hereditary Spastic Paraplegia type 6 (SPG6), a neurological disorder characterized by progressive weakness and spasticity of the legs. Understanding the symptoms associated with the NIPA1 gene mutation is crucial for early diagnosis and management of the condition. DNA […]
In the realm of genetic research and testing, the identification and understanding of specific genes and their associated conditions have opened up new avenues for diagnosis and treatment. One such gene that has garnered attention is the WDR48 gene, which is linked to a condition known as SPG60. DNA Labs UAE, a leading genetic laboratory, […]
In the rapidly advancing field of genetic diagnostics, the identification of specific genes responsible for inherited disorders has become a cornerstone of personalized medicine. Among these genetic markers, the ARL6IP1 gene has garnered attention for its role in SPG61, a rare form of hereditary spastic paraplegia. DNA Labs UAE is at the forefront of providing […]
Sure, here’s a detailed article structured as requested: — Understanding AP4B1 Gene and SPG47 The AP4B1 gene is crucial for human biology, playing a significant role in the development and function of the central nervous system. Mutations in this gene can lead to a rare and complex form of spastic paraplegia, known as SPG47. This […]
Understanding the complexities of genetic conditions is a crucial aspect of modern healthcare. One such condition that has garnered attention is associated with mutations in the ERLIN1 gene, known as SPG62. This condition falls under the umbrella of hereditary spastic paraplegias (HSP), a group of genetic disorders characterized by progressive weakness and spasticity of the […]
Understanding the AP5Z1 Gene and SPG48 Genetic Test The AP5Z1 gene is crucial in the understanding of a rare neurological disorder known as Spastic Paraplegia 48 (SPG48). This condition, inherited in an autosomal recessive manner, leads to a range of symptoms that can significantly impact an individual’s quality of life. To diagnose this condition accurately, […]
Understanding the AMPD2 Gene and SPG63 Genetic Test The AMPD2 gene is a critical component of our genetic makeup, playing a significant role in the development and function of our nervous system. Mutations in this gene have been linked to a rare neurological disorder known as Spastic Paraplegia 63 (SPG63). This condition is characterized by […]
— The TECPR2 gene is associated with a rare neurological disorder known as Spastic Paraplegia 49 (SPG49). This condition is part of a group of disorders known as Hereditary Spastic Paraplegias (HSPs), which are characterized by progressive weakness and spasticity of the legs. SPG49, caused by mutations in the TECPR2 gene, is a complex form […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
