In cases of de novo genetic alterations, the genetic changes are not passed down by the parents, but are present for the first time in the patient. Genetic panel means that several genes known to be associated with a certain syndrome are sequenced simultaneously. Therefore, this website places "cookies" onto your computer to collect information about your use of our site. Genetic testing is most often done to confirm the diagnosis of a syndrome or disease, which is known to be caused by a genetic alteration. This approach is most often used if the syndrome/symptoms are not known in the family and do not point to one specific syndrome. The detected variants are analyzed and evaluated by an experienced team of scientists and geneticists and summarized in a comprehensive medical report. 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. Generating a clean environment to live, by assessing causes of health-problems and cancer. Learn more how genetic testing in Dubai can help you achieve your health goals. The main focus is to establish different medical DNA diagnostic and cancer research programs with the objectives of acting as the major player in the expanding arena of human safety and health, preventive medicine and improving the current status of cancer programs in Dubai (UAE), by generating a network of excellence, and implementing personalized medicine programs. Please click on the ok button to consent to the use of cookies on this website. The cost increases if more than one test is necessary or if multiple family members must be tested to obtain a meaningful result. The outcomes shall lead to make Dubai and other cities in UAE healthiest place(s) to live in! Location. Book your appointment now! 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). To generate a Network of Medical Excellence in Dubai (UAE). Genetic testing is also common in the Emirates and every UAE national must be screened before marrying. Sign up now to receive latest updates from the hospital, Copyright © 2020 Iranian Hospital - Dubai, To set up a DNA Diagnostic Medical Center, To improve the detection limit for cancer, Pre-cancers screening tests for monitoring of UAE national and residents, Pre-screening tests for non-cancer human diseases for monitoring of UAE national and residents, To implement personalized medicine for cancer and non-cancer patients. Reach out to us now! See our PRIVACY POLICY statement for details and COOKIE POLICY on how they work. Preimplantation genetic diagnosis (PGD), mostly referred to now as preimplantation genetic testing for monosomic diseases/single-gene disorders (PGT, or more formally PGT-M), utilizes state-of-the-art fertility techniques such as in vitro fertilization, embryo biopsy, and customized genetic testing to implant embryos free from certain disease gene(s). The outcomes consequently may lead to preventive medicine. Moreover, Dubai will become a center of reference for the rest of Arab world inhabitants for performing DNA diagnostic tests, and other medical cares in relation to preventive medicine and personalized cancer therapy regimen. These genetic changes can either be hereditary or occur de novo (for the first time). Genetic Counselling Dubai - Iranian Hospital is one of the best Genetic Clinics in Dubai, UAE provides counselling, testing, evaluation, diagnosis and treatment for a variety of genetic disorders. We want to ensure that you enjoy browsing our website and have a performant experience. For newborn screening, costs vary by state. The price of direct-to-consumer genetic testing ranges from under a hundred dollars to several thousand dollars. LAB HOURS: SAT - THU : 9:00 AM to 9:00 PM, Medical Advertisement - Ministry of Health License No. Paving the way toward setting up personalized medicine. In order to achieve these objectives the following platforms are being assembled, as follows: The outcomes shall generate utmost health prosperities for the people living in Dubai (UAE), and lead to make Dubai a reference center on DNA diagnostic and Cancer programs. Often, in cases of hereditary genetic alterations, the syndrome/symptoms are known in the family and one or more relatives may have previously been diagnosed with this genetic change. The cost of genetic testing can range from under $100 to more than $2,000, depending on the nature and complexity of the test. MF05059 – valid upto 14.06.2021. In a genetic panel, many genes involved in specific or unspecific symptoms can be tested at once. Usually, in these cases, the doctor/geneticist will suspect a syndrome based on the symptoms and other tests, and order the genetic test for confirmation. Depending on the syndrome/symptoms, the number of associated genes may vary. Some states cover part of the total cost, but most charge a fee of $15 to $60 per infant. 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).