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آزمایشگاه ژنتیک پزشکی سیتوژن

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    • چهارراه باغشمال، خ باغشمال، مجتمع پزشکان باغشمال
    • 041-35576215
    • cytogene_lab@yahoo.com
    آزمایشگاه ژنتیک پزشکی سیتوژن
    • cytogene_lab@yahoo.com
    • چهارراه باغشمال، خ باغشمال، مجتمع پزشکان باغشمال
    • دریافت نوبت
    • درباره سیتوژن
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    • مشاوره ژنتیک
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      • مشاوره ژنتیک سرطان
      • مشاوره ناباروری‌ و‌ سقط مکرر
    • خدمات
      • تشخیص پیش کاشتی
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      • تشخیص علل سقط‌‌ مکرر
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      • تشخیص و غربال‌گری سرطان
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    اطلاعات تماس

    • تبریز، باغشمال، ساختمان هلیا، طبقه دوم
    • 04135576215
    • cytogene_lab@yahoo.com

    پانل‌های بیماری

      آزمایشگاه ژنتیک پزشکی سیتوژن > راهنمای پزشکان > پانل‌های بیماری

    قلب و عروق (Cardiology)

    Aorta Panel
    Arrhythmia Panel
    Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel
    Atrial Fibrillation Panel
    Brugada Syndrome Panel
    Cardiomyopathy Panel
    Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
    Comprehensive Cardiology Panel
    Congenital Structural Heart Disease Panel
    Dilated Cardiomyopathy (DCM) Panel
    Ehlers-Danlos Syndrome Panel
    Hereditary Hemorrhagic Telangiectasia (HHT) Panel
    Heterotaxy and Situs Inversus Panel
    Hyperlipidemia Core Panel
    Hyperlipidemia Panel
    Hypertrophic Cardiomyopathy (HCM) Panel
    Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel
    Liddle Syndrome Panel
    Long QT Syndrome (LQTS) Panel
    Marfan Syndrome Panel
    Noonan Syndrome Panel
    Pulmonary Artery Hypertension (PAH) Panel
    Short QT Syndrome (SQTS) Panel

    پوست، مو و ناخن (Dermatology)

    Adams-Oliver Syndrome Panel
    Albinism Panel
    Cutis Laxa Panel
    Dyskeratosis Congenita Panel
    Ectodermal Dysplasia Panel
    Ehlers-Danlos Syndrome Panel
    Epidermolysis Bullosa Panel
    Hereditary Acrodermatitis Enteropathica Panel
    Hereditary Melanoma and Skin Cancer Panel
    Hermansky-Pudlak Syndrome Panel
    Ichthyosis Panel
    Neurofibromatosis Panel
    Pachyonychia Congenita Panel
    Palmoplantar Keratoderma Panel
    Progeria and Progeroid Syndromes Panel
    Tuberous Sclerosis Panel
    Waardenburg Syndrome Panel
    Xeroderma Pigmentosum Panel

    گوش، حلق و بینی (Ear, Nose & Throat)

    Alport Syndrome Panel
    Branchio-Oto-Renal (BOR) Syndrome Panel
    Comprehensive Hearing Loss and Deafness Panel
    Hereditary Hemorrhagic Telangiectasia (HHT) Panel
    Non-Syndromic Hearing Loss Panel
    Pendred Syndrome Panel
    Resonate Program Panel
    Stickler Syndrome Panel
    Syndromic Hearing Loss Panel
    Usher Syndrome Panel
    Waardenburg Syndrome Panel

    غدد درون‌ریز و متابولیسم (Endocrinology)

    Abnormal Genitalia/ Disorders of Sex Development Panel
    Comprehensive Monogenic Diabetes Panel
    Congenital Adrenal Hyperplasia Panel
    Glucocorticoid Deficiency Panel
    Hyperlipidemia Panel
    Hyperparathyroidism Panel
    Hypoglycemia, Hyperinsulinism and Ketone Metabolism Panel
    Hypomagnesemia Panel
    Hypothyroidism and Resistance to Thyroid Hormone Panel
    Kallmann Syndrome Panel
    MODY Panel
    Monogenic Obesity Panel
    Premature Ovarian Failure Panel

    گوارش (Gastroenterology)

    Cholestasis Panel
    Congenital Diarrhea Panel
    Congenital Hepatic Fibrosis Panel
    Gastrointestinal Atresia Panel
    Hirschsprung Disease Panel
    Pancreatitis Panel
    Polycystic Liver Disease Panel

    خون شناسی (Hematology)

    Anemia Panel
    Bleeding Disorder/Coagulopathy Panel
    Bone Marrow Failure Syndrome Panel
    Coagulation Factor Deficiency Panel
    Comprehensive Hematology and Hereditary Cancer Panel
    Comprehensive Hematology Panel
    Comprehensive Immune and Cytopenia Panel
    Congenital Neutropenia Panel
    Diamond-Blackfan Anemia Panel
    Dyskeratosis Congenita Panel
    Fanconi Anemia Panel
    Hemophagocytic Lymphohistiocytosis Panel
    Hereditary Leukemia Panel
    Hermansky-Pudlak Syndrome Panel
    Platelet Function Disorder Panel
    Red Blood Cell Membrane Disorder Panel
    Thrombocytopenia Panel

    نشانگان سرطان (Hereditary Cancer)

    Comprehensive Hematology and Hereditary Cancer Panel
    Comprehensive Hereditary Cancer Panel
    Hereditary Breast and Gynecological Cancer Panel
    Hereditary Breast Cancer High Risk Panel
    Hereditary Cancer High Risk Panel
    Hereditary Colorectal Cancer Panel
    Hereditary Endocrine Cancer Panel
    Hereditary Gastrointestinal Cancer Panel
    Hereditary Leukemia Panel
    Hereditary Lung Cancer Panel
    Hereditary Melanoma and Skin Cancer Panel
    Hereditary Pancreatic Cancer Core Panel
    Hereditary Pancreatic Cancer Panel
    Hereditary Paraganglioma-Pheochromocytoma Panel
    Hereditary Pediatric Cancer Panel
    Hereditary Renal Cancer Panel
    Neurofibromatosis Panel
    Tuberous Sclerosis Panel
    Xeroderma Pigmentosum Panel

    ایمونولوژی (Immunology)

    Autoinflammatory Syndrome Panel
    Bone Marrow Failure Syndrome Panel
    Chronic Granulomatous Disease Panel
    Complement System Disorder Panel
    Comprehensive Immune and Cytopenia Panel
    Congenital Neutropenia Panel
    Dyskeratosis Congenita Panel
    Hemophagocytic Lymphohistiocytosis Panel
    Primary Immunodeficiency (PID) and Primary Ciliary Dyskinesia (PCD) Panel
    Primary Immunodeficiency Panel
    Severe Combined Immunodeficiency Panel

    نقص عضو و معلولیت (Malformations)

    3-M Syndrome / Primordial Dwarfism Panel
    Adams-Oliver Syndrome Panel
    Amelogenesis Imperfecta and Dentinogenesis Imperfecta Panel
    Arthrogryposes Panel
    Brachydactyly / Syndactyly Panel
    Cerebral Cavernous Malformation Panel
    Chondrodysplasia Punctata 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
    Cornelia de Lange Syndrome Panel
    Craniosynostosis Panel
    Exostosis and Related Disorders Panel
    Facial Dysostosis and Related Disorders Panel
    Gastrointestinal Atresia Panel
    Heterotaxy and Situs Inversus Panel
    Hirschsprung Disease Panel
    Holoprosencephaly Panel
    Kabuki Syndrome Panel
    Limb Malformations Panel
    Lissencephaly Panel
    Lymphatic Malformations and Related Disorders Panel
    Macrocephaly / Overgrowth Syndrome Panel
    Meier-Gorlin Syndrome Panel
    Metaphyseal Dysplasia Panel
    Microcephaly and Pontocerebellar Hypoplasia Panel
    Micromelic Dysplasia Panel
    Neurofibromatosis Panel
    Neuronal Migration Disorder Panel
    Osteogenesis Imperfecta Panel
    Osteopetrosis and Dense Bone Dysplasia Panel
    Polymicrogyria Panel
    Seckel Syndrome Panel
    Septo-Optic Dysplasia Panel
    Short Rib Dysplasia / Asphyxiating Thoracic Dysplasia Panel
    Skeletal Dysplasia with Abnormal Mineralization Panel
    Skeletal Dysplasias Core Panel
    Spondylometaphyseal / Spondyloepi-(meta)-physeal Dysplasia Panel
    Vascular Malformations Panel

    اختلالات متابولیک (Metabolic Disorders)

    Aicardi-Goutières Syndrome Panel
    Coenzyme q10 Deficiency Panel
    Comprehensive Metabolism Panel
    Congenital and Familial Lipodystrophy Panel
    Congenital Disorders of Glycosylation Panel
    Congenital Mono- and Disaccharide Disorders Panel
    Creatine Metabolism Deficiency Panel
    Cystinuria Panel
    Fatty Acid Oxidation Syndrome Panel
    Glycogen Storage Disorder Panel
    Hereditary Hemochromatosis Panel
    Homocystinuria Core Panel
    Hyperammonemia and Urea Cycle Disorder Panel
    Hyperphenylalaninemia Panel
    Hypoglycemia, Hyperinsulinism and Ketone Metabolism Panel
    Hypomagnesemia Panel
    Lysosomal Disorders and Mucopolysaccharidosis Panel
    Metabolic Liver Failure Panel
    Metabolic Myopathy and Rhabdomyolysis Panel
    Mitochondrial DNA Depletion Syndrome Panel
    Monogenic Obesity Panel
    Nephrolithiasis Panel
    Nonketotic Hyperglycinemia / Glycine Encephalopathy Panel
    Organic Acidemia/Aciduria & Cobalamin Deficiency Panel
    Periodic Paralysis Panel
    Peroxisomal Disorders Panel
    Porphyria Panel
    Purine and Pyrimidine Metabolism Disorders Panel
    Tyrosinemia Panel

    اختلالات آنزیم‌ها (Mitochondrial Disorders)

    Mitochondrial DNA Depletion Syndrome Panel
    Mitochondrial Genome Test

    کلیه (Nephrology)

    Alport Syndrome Panel
    Bardet-Biedl Syndrome Panel
    Bartter Syndrome Panel
    Branchio-Oto-Renal (BOR) Syndrome Panel
    Ciliopathy Panel
    Cystic Kidney Disease Panel
    Diabetes Insipidus Panel
    Hemolytic Uremic Syndrome Panel
    Hypomagnesemia Panel
    Hypophosphatemic Rickets Panel
    Joubert Syndrome Panel
    Liddle Syndrome Panel
    Meckel Syndrome Panel
    Monogenic Obesity Panel
    Nephrolithiasis Panel
    Nephronophthisis Panel
    Nephrotic Syndrome Panel
    Polycystic Kidney Disease Panel
    Primary Ciliary Dyskinesia Panel
    Primary Hyperoxaluria Panel
    Pseudohypoaldosteronism Panel
    Renal Malformation Panel
    Renal Tubular Acidosis Panel
    Senior-Loken Syndrome Panel

    عصب شناسی (Neurology)

    Amyotrophic Lateral Sclerosis Panel
    Ataxia Panel
    Autism Spectrum Disorders Panel
    Beyond Paediatric Epilepsy Panel – for Europe and Middle East
    Cerebral Cavernous Malformation Panel
    Charcot-Marie-Tooth Neuropathy Panel
    Coenzyme q10 Deficiency Panel
    Collagen Type VI-Related Disorders Panel
    Comprehensive Epilepsy Panel
    Comprehensive Muscular Dystrophy / Myopathy Panel
    Congenital Myasthenic Syndromes Panel
    Creatine Metabolism Deficiency Panel
    Dementia Panel
    Dystonia Panel
    Emery-Dreifuss Muscular Dystrophy Panel
    Epileptic Encephalopathy Panel
    Holoprosencephaly Panel
    Idiopathic Generalized and Focal Epilepsy Panel
    Leukodystrophy and Leukoencephalopathy Panel
    LGMD and Congenital Muscular Dystrophy Panel
    Lissencephaly Panel
    Macrocephaly / Overgrowth Syndrome Panel
    Metabolic Epilepsy Panel
    Metabolic Myopathy and Rhabdomyolysis Panel
    Microcephaly and Pontocerebellar Hypoplasia Panel
    Migraine Panel
    NCL and Progressive Myoclonic Epilepsy Panel
    Nemaline Myopathy Panel
    Neuro-Ophthalmology Panel
    Neuronal Migration Disorder Panel
    Parkinson Disease Panel
    Periodic Paralysis Panel
    Polymicrogyria Panel
    Porphyria Panel
    Septo-Optic Dysplasia Panel
    Spastic Paraplegia Panel
    Spinal Muscular Atrophy Panel
    Tuberous Sclerosis Panel
    X-linked Intellectual Disability Panel

    چشم (Ophthalmology)

    Achromatopsia Panel
    Albinism Panel
    Bardet-Biedl Syndrome Panel
    Cataract Panel
    Cone Rod Dystrophy Panel
    Congenital Stationary Night Blindness Panel
    Corneal Dystrophy Panel
    Ectopia Lentis Panel
    Flecked Retina Disorders Panel
    Glaucoma Panel
    Joubert Syndrome Panel
    Leber Congenital Amaurosis Panel
    Macular Dystrophy Panel
    Microphthalmia, Anophthalmia and Anterior Segment Dysgenesis Panel
    My Retina Tracker Program Panel
    Neuro-Ophthalmology Panel
    Optic Atrophy Panel
    Retinal Dystrophy Panel
    Retinitis Pigmentosa Panel
    Senior-Loken Syndrome Panel
    Septo-Optic Dysplasia Panel
    Stickler Syndrome Panel
    Usher Syndrome Panel
    Vitreoretinopathy Panel

    ریه (Pulmonology)

    Bronchiectasis Panel
    Central Hypoventilation and Apnea Panel
    Comprehensive Pulmonology Panel
    Cystic Lung Disease Panel
    Hermansky-Pudlak Syndrome Panel
    Interstitial Lung Disease Panel
    Neonatal Respiratory Distress – Surfactant Dysfunction Panel
    Primary Ciliary Dyskinesia Panel
    Pulmonary Artery Hypertension (PAH) Panel

    آزمایشگاه ژنتیک پزشکی سیتوژن

    سیتوژن؛ به‌روزترین و جامع‌ترین آزمایشگاه ژنتیک پزشکی شمال‌غرب کشور

    • تبریز، چهارراه باغشمال،
      خیابان باغشمال
      مجتمع پزشکان باغشمال
    • شماره‌‎ تماس: 35578432-041
    • cytogene_lab@yahoo.com

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    • درباره سیتوژن
    • بخش‌های آزمایشگاه
    • مشاوره ژنتیک و بالینی
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    • پانل‌های بیماری
    • سیتومگ

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