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  BioMatrix, with its experienced team of professionals, can provide complete solution for analytical laboratories by equipping, building human resources capacities, transferring of the know-how, launching the project, follow-up on management and on accreditation requirements.  



Diagnostic Laboratories
Clinical diagnostic laboratories provide routine and specialty testing of body fluids in clinical chemistry, hematology, serology, endocrinology, bacteriology, virology and parasitology fields.



Genetic Diagnosis
DNA testing facilities diagnoses genetically inherited disorders including prenatal diagnosis, newborn genetic screening and genetic predictive medicine.


Such as Trisomy (Down syndrome), Monosomy (Turner syndrome), Uniparental Disomy
(Also called Mendelian or monogenic) such as Cystic Fibrosis, Sickle Cell Anemia.
Such as, Gene Mutations, Tumor markers, Breast cancer, Colon Cancer
(Also called complex or polygenic) such as Alzheimer’s disease, arthritis, diabetes, cancer, and obesity
Such as Diabetes Mellitus, Deafness, Multiple Sclerosis MS, Neuropathy, Ataxia, Retinitis Pigmentosa, Ptosis



Cord Stem Cell Banking
Stem Cell Banking offers once-in-a-lifetime opportunity to preserve newborns’ stem cells in high-tech cellular cryogenic compartments for potential future use.


Neonatal Screening
Neonatal screening laboratories test for inborn errors of metabolism that cause serious physical or mental handicaps if not early detected and treated.


Metabolic disorders result from inherited deficiencies in cell enzymatic activities and cause serious physical or mental handicaps. An early detection and treatment of these disorders will prevent these handicaps.
Ministries of health in the majority of developed countries are implementing mandatory neonatal screening on newborns.
By acquiring the know-how and the technology, hospitals and laboratories can diagnose more than 40 metabolic diseases in less than 2 minutes. Covering mainly:
Cystic fibrosis
Blood Cell Disorders (Hemoglobinopathies)
Hemoglobin C Disorder
Hemoglobin O Arab Disorder
Hemoglobin E Disorder
Hemoglobin D Disorder
Sickle cell anemia
Amino Acids Disorders   
Argininosuccinase Deficiency (Argininosuccinase Aciduria)
Argininosuccinic Synthetase Deficiency (Citrullinemia) Type I
Phenylketonuria/ Hyperphenylalaninemia
Maple Syrup Urine Disease (MSUD)
Homocystinuria/ Hypermethioninemia
Argininosuccinic Synthetase Deficiency (Citrullinemia) Type II
Organic Acids Disorders   
Glutaric Acidemia type I (GA-I)
3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency (HMG)
Isovaleric Acidemia (IVA)
Methylcrotonyl-CoA carboxylase Deficiency (MCC)
Methylmalonyl-CoA mutase deficiency ("MUT")
Methylmalonic Acidemia (MMA, Different types)
3-ketothiolase Deficiency (BKT)
Propionic Acidemia (PA)
Multiple CoA Carboxylase Deficiency (MCD)
Fatty Acid Oxidation Defects   
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
Short-chain acyl-CoA dehydrogenase Deficiency (SCAD)
Ethylmalonic Aciduria (EMA)
Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
3-Hydroxy-Long-Chain Acyl-CoA Dehydrogenase Deficiency (LCHAD)
Glutaric acidemia Type-II (GA-II; MADD)
Carnitine transporter deficiency
Carnitine palmitoyltransferase Deficiency type I (CPTI)
Carnitine palmitoyltransferase Deficiency type II (CPTII)
Carnitine-acylcarnitine translocase Deficiency (trans)


Stem cell therapy is a revolutionary and promising medical technology that would be a major investment in the medical field for the coming decades.
Stem cells are master cells that have the capability to form any or all of an individual's tissues and organs. These cells are instrumental in the fight against diseases such as Leukemia, Lymphomas, Diabetes, Osteoporosis, CVA, Parkinson's, Liver and Heart Diseases.

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