Lab Tests Directory
Browse our comprehensive catalog of medical tests. Book online and get tested at home or at a licensed lab in Dubai and Sharjah.
Microarray 315k (Products of conception)
This blood test uses microarray technology to analyze genetic material, often in cases related to products of conception (tissue from miscarriage or stillbirth). It helps identify chromosomal abnormalities that may have contributed to pregnancy loss.
Microsporidium Detection by smear examination
This test involves a microscopic examination of a stool sample to detect the presence of Microsporidium parasites. These tiny organisms can cause gastrointestinal infections.
Mitochondrial DNA Sequencing
This blood test analyzes the entire genetic material found within your mitochondria, the "powerhouses" of your cells. It looks for specific mutations that can cause mitochondrial disorders.
MOLYBDENUM
This blood test measures the level of Molybdenum, an essential trace mineral, in your body. Molybdenum plays a crucial role in various bodily functions, including enzyme activity.
MRSA (Methicillin Resistant Staphylococcus aureus) DNA Detection by PCR
This test uses PCR technology to detect the DNA of Methicillin-Resistant Staphylococcus aureus (MRSA) from a swab sample. MRSA is a type of staph bacteria that is resistant to several common antibiotics.
MTHFR (C677T and 1298C) GENE MUTATION, QUALITATIVE
This test identifies specific genetic variations (mutations) in the MTHFR gene, specifically C677T and A1298C. These mutations can affect how your body processes folate (Vitamin B9), which is vital for many bodily functions, including DNA synthesis and repair.
Mucopolysaccharides (MPS) Type-I
This test screens for Mucopolysaccharidosis Type I (MPS I), a rare genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase. This enzyme is essential for breaking down complex sugars (mucopolysaccharides) in the body.
Mucopolysaccharides (MPS) Type-VI
This test screens for Mucopolysaccharidosis Type VI (MPS VI), also known as Maroteaux-Lamy syndrome. It's a rare genetic disorder caused by a deficiency in the enzyme N-acetylgalactosamine-4-sulfatase, which is vital for breaking down specific complex sugars.
Mucopolysaccharides (MPS) Typing
This test analyzes urine for specific types of mucopolysaccharides, which are complex sugar molecules. It helps identify and classify different forms of mucopolysaccharidosis, a group of rare genetic disorders.
MuSK (MUSCLE SPECIFIC KINASE) ANTIBODY
This blood test detects antibodies against Muscle Specific Kinase (MuSK), a protein crucial for nerve-muscle communication. The presence of these antibodies is often associated with a specific form of myasthenia gravis.
NF1 Gene Deletion and Duplication by MLPA
This genetic test uses MLPA (Multiplex Ligation-dependent Probe Amplification) to detect deletions or duplications within the NF1 gene. Changes in this gene are associated with Neurofibromatosis Type 1, a genetic disorder affecting nerve tissue growth.
NGS COUPLE CARRIER SCREENING + DMD+SMA
This advanced Next-Generation Sequencing (NGS) test screens couples for a broad range of genetic conditions, including specific screening for Duchenne Muscular Dystrophy (DMD) and Spinal Muscular Atrophy (SMA). It provides a comprehensive risk assessment for genetic disorders that could be passed to offspring.