Book your appointment now! SAT - THU 9:00 AM to 9:00 PM | FRIDAY : Closed, Copyright © 2020 All rights reserved | FREIBURG MEDICAL LABORATORY MIDDLE EAST (L.L.C). The cost increases if more than one test is necessary or if multiple family members must be tested to obtain a meaningful result. These genetic changes can either be hereditary or occur de novo (for the first time). Schedule an appointment by calling us at +971 4 243 4166 or sending us an email at [email protected] You can also fill up our online contact form for easier communication. You have questions or want to meet our therapists to start your journey? The cost depends on how many genetic variations are analyzed (and it will cost more if whole genome or whole exome sequencing is used), how extensive the interpretation of results is, and whether other products, programs, or services are included. We want to ensure that you enjoy browsing our website and have a performant experience. In order to achieve these objectives, updated and state of the art cytogenetic assays (including whole gnome analysis using chromosome painting) and DNA molecular biology assays (including next generation sequencing) will be introduced and implemented to access frequencies of spontaneously occurring as well as induced chromosomal alterations, by physical (such as radiation of different qualities) and chemical (such as pollutants and human hazardous in air, soil, water and food) agents, These studies can be complimented with analyzing whole genome (DNA, protein and enzymes). Consequently, a huge sum of money that on a regular basis in the last so many years for medical cares is spent by the UAE national out of the UAE, can be saved. Please send us an email with the name of the syndrome/disorder or gene and we will send you the details (price, TAT, additional info) of the required test. Genetic testing allows the patient to confirm his/her diagnosis. Epilepsy & Brain Development Disorders Gene Panels, Mitochondrial DNA Testing - Mitochondriopathies Gene Panels, MLPA (Multiplex ligation-dependent probe amplification), aCGH – Array comparative genomic hybridization, Genetic Counseling (Pre-Test and Post-Test), G6PDH and HLA B27 -- New In-House Test at FML, H. pylori Culture and Sensitivity Testing, Hearing Loss, mitochondrial, including aminoglycoside ototoxicity, Hearing Loss, nonsyndromic, autosomal dominant and X-linked, Hearing Loss, nonsyndromic, autosomal recessive and X-linked, VB12-dependent Megaloblastic Anemia Panel, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel, Cardiomyopathy with onset in neonatal period, infancy or childhood panel, Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel, Congenital Structural Heart Disease Panel, Hereditary Hemorrhagic Telangiectasia (HHT) Panel, Hypercholesterolemia and Hyperlipoproteinemia Panel, Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel, Neuromuscular disease with Cardiomyopathy Panel, Pulmonary Artery Hypertension (PAH) Panel, Ehlers-Danlos Syndrome, Marfan Syndrome, Loeys-Dietz Syndrome, Aortic Aneurysm and Differential Diagnoses Panel, Ectodermal dysplasia, selective tooth agenesis, richothiodystrophy, and hypotrichosis panel, Hereditary Acrodermatitis Enteropathica Panel, Hereditary Melanoma and Skin Cancer Panel, Hyperpigmentation: Dowling-Degos disease and related disorders panel, Ichthyosis, palmoplantar keratoderma, and related disorders of cornification panel, Photodermatosis: Xeroderma pigmentosum, Cockayne syndrome, COFS syndrome and related disorders panel, Syndromic albinism and related disorders: Hermansky-Pudlak syndrome, Griscelli syndrome, Waardenburg syndrome panel, Vascular disorders: hereditary hemorrhagic telangiectasia, cerebral cavernous malformations, association with MoyaMoya, and related disorders panel, Comprehensive Hearing Loss and Deafness Panel, Epilepsy and Developmental Delay (including Epileptic Encephalopathies) Panel, GPI anchor deficiency with or without Hyperphosphatasia Panel, Progressive Myoclonus Epilepsy and Neuronal Ceroid Lipofuscinosis Panel, Leukodystrophy/Leukoencephalopathy and Differential Diagnoses, Microcephaly and Pontocerebellar Hypoplasia, Abnormal Genitalia/Disorders of Sex Development Panel, Hypoglycemia, Hyperinsulinism and Ketone Metabolism Panel, Hypothyroidism and Resistance to Thyroid Hormone Panel, Hereditary Breast and Gynecological Cancer Panel, Hereditary Paraganglioma-Pheochromocytoma Panel, Complement System Disorder/Compliment Deficiencies Panel, Primary Immunodeficiency (PID) and Primary Ciliary Dyskinesia (PCD) Panel, Hypercholanemia and defects of bile acid synthesis, Impairments of transport in hepatocytes and cholangiocytes panel, Metabolic disorders of hepatocytes, including Tyrosinemia, Glycogen storage diseases,Hyperammonemia, Shwachman-Diamond syndrome, Disorder of fatty acid oxidations and Peroxisomal diseases, Amelogenesis Imperfecta and Dentinogenesis Imperfecta Panel, Cleft Lip/Palate and Associated Syndromes Panel, Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel, Comprehensive Short Stature Syndrome Panel, Comprehensive Skeletal Dysplasias and Disorders Panel, Facial Dysostosis and Related Disorders Panel, Lymphatic Malformations and Related Disorders Panel, Microcephaly and Pontocerebellar Hypoplasia Panel, Osteopetrosis and Dense Bone Dysplasia Panel, Short Rib Dysplasia/Asphyxiating Thoracic Dysplasia Panel, Skeletal Dysplasia with Abnormal Mineralization Panel, Spondylometaphyseal/Spondyloepi-(meta)-physeal Dysplasia Panel, Congenital and Familial Lipodystrophy Panel, Congenital Disorders of Glycosylation (CDG syndrome) Panel, Congenital Mono- and Disaccharide Disorders Panel, Hyperammonemia and Urea Cycle Disorder Panel, Maple Syrup Urine Disease and DLD Deficiency Panel, Maturity-onset Diabetes of the Young (MODY) Panel, Metabolic Myopathy and Rhabdomyolysis Panel, Mitochondrial DNA Depletion Syndrome Panel, Molybdenum Cofactor and Sulfite Oxidase Deficiency Panel, Nonketotic Hyperglycinemia/Glycine Encephalopathy Panel, Organic Acidemia/Aciduria & Cobalamin Deficiency Panel, Peroxisome Biogenesis Disorders: Zellweger spectrum disorder panel, Purine and Pyrimidine Metabolism Disorders Panel, Pyridoxine- and Folic Acid-dependent epilepsy panel, Comprehensive Muscular Dystrophy/Myopathy Panel, Idiopathic Generalized and Focal Epilepsy Panel, Leukodystrophy and Leukoencephalopathy Panel, LGMD and Congenital Muscular Dystrophy Panel, NCL and Progressive Myoclonic Epilepsy Panel, Congenital Stationary Night Blindness Panel, Microphthalmia, Anophthalmia and Anterior Segment Dysgenesis Panel, Ocular malformations panel (microphthalmia/anophthalmia/nanophthalmia/ coloboma), Stargardt disease and macular dystrophies panel, Syndromic albinism (Hermansky-Pudlak/Waardenburg/Vici/ Griscelli), Vitreoretinopathies (Wagner syndrome/Norrie/Coats), Zellweger syndrome spectrum (Refsum/Zellweger/neonatale adrenoleukodystrophy), Neonatal Respiratory Distress – Surfactant Dysfunction Panel, Achondroplasia, Hypochondroplasia, and Pseudoachondroplasia Panel, Cleidocranial dysplasia and related disorders panel, Craniofacial and patellar dysostoses; dysostoses with vertebral and costal inolvement: Klippel-Feil syndrome, Meier-Gorlin syndrome, and related disorders panel, Hypophosphatemic rickets and related skeletal dysplasias with abnormal mineralization panel, Limb malformations: isolated brachydactyly, synostoses, split-hand/foot, polydactyly, syndactyly, and selected genetic syndromes with limb malformations panel, Lysosomal storage disorders with skeletal involvement panel, Micromelic dysplasia: acromelic, acromesomelic, mesomelic and rhizo-mesomelic dysplasia panel, Multiple epiphyseal dysplasia and pseudoachondroplasia panel, Osteogenesis imperfecta and related skeletal dysplasias with decreased bone density panel, Osteopetrosis and related skeletal dysplasias with increased bone density panel, Potentially lethal skeletal disorders panel, Seckel syndrome, 3-M syndrome, Rubinstein–Taybi syndrome, Kabuki syndrome, and further selected genetic syndromes with skeletal involvement panel, Spondylometaphyseal dysplasia and Spondylo-epi-(meta)-physeal dysplasia panel, Nuclear encoded mitochondrial diseases–359 Genes, Mitochondrial encephalopathy/Mitochondrial Hepato(encephalo)pathy, Mitochondrial DNA-depletion and deletion syndromes, Combined oxidative phosphorylation deficiency, CoQ10 Deficiency and Acyl-CoA-Dehydrogenase Deficiency, Progressive external ophthalmoplegia(PEO/CPEO).


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