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قابل توجه کسانی که سابقه بیماری رنتیکی در خانواده خود دارند 


با استفاده از روش ای وی اف میتوان از عدم انتقال بیماریهای زنتیکی زیر به جنین اطمینان حاصل کرد




2. Single Gene Disorder: Autosomal recessive, Autosomal dominant and X-Linked
Achondroplasia
Adenosine Deaminase Deficiency
Adrenal Hyperplasia
Alagille Syndrome
Albinism
Alpha Thalassemia
Ataxia Telangectasia
Auto-immune Lymphoprolepherative Syndrome
Beckwith-Wiedernmann Syndrome
Beta Thalassemia, Sickle Cell Anemia
Bilateral Lebers Congenital Amaurosis
Biotidinase Deficiency
Blindness (Usher syndrome)
Brakytachtyly Type B
CADASIL
Carbohydrate-Deficient Glycoprotein Syndrome, Type I
Charcot-marie Tooth Disease
Congenitail Adrenal Hyperplasia
Congenitail Cholestosis
Congenital Analgesia Syndrome
Congenital Disorder of Glycosylation
Congenital Icthysosis
Congenital Mytonia
Congenital Nephrosis
Criggler Najjar Syndrome
Cystic Fibrosis
Deafness (Connexin 26)
Duchenne Backet Muscular Dystrophy
Ehler Donlos Syndrome
Epidermolysis Bullosa
Fabrys Disease
Familial Juvenile Nephrosis
Familial Meditteranian Fever Disease
Fanconi Anemia
Fragile X Syndrome
Friedreich Ataxia
Fructose 1,6 Biphosphate
Glucose 6 Phosphate Dehydrogenase
Gaucher Disease
Glutaric Aciduria type1,2,3
Glycosyl Decarboxylase (GLDC,AMH)
Hemachromatosis
Hemophilia
Heraditary Spastic Paraparesis
Huler-schei Syndrome
Hurler Syndrome (Type 1)
Hyperoxaluria
Icythyosis
Infartile Polycystic Kidney Disease
Insulin-Dependent Diabetes Mellitus (type 1 diabetus mellitus)
Isovaleric Aciduria
Joubert Syndrome
K-Ras Mutation screening
Lamellar Ichosis
Leucodystrophia
Leukocyte Adhesion syndrome
Lipoprotein lipase syndrome
Maple Syrup Urine Disease
Marfan Syndrome
Maturity-onset diabetes of the young
Meckel Gruber Syndrome
Medium Chain acyl CoA Dehydrogenase
Methylene Tetrahydrofolate Reductase
Methylmalonic Acidemia
Mitochondrial genome screening
Mucopolysaccharidosis TYPE I
Mucopolysaccharidosis-Type III
Mucopolysaccharidosis-Type IV
Mucopolysaccharidosis-Type VI
Multiple Acyl coA deficiency
Multiple Endocrine Neoplasia-Type1
Neiman-pick Type B
Neonatal Cholestasis
Neurofibromatosis
Neuronal Ceroid Lipopherosis
Nevoid Basal Cell Carcinoma Syndrome
Non Polyposis Colon Cancer
Non-Insulin Dependent Diabetes
Noonan Syndrome
Omenn Syndrome
Ornithine Transcarbomylase Deficiency
Osteogenesis Imperfecta
Osteopetrosis
Paroxymal Biogene Disorder
Perforin
PhenylKetonuria
Polycythemia Vera
Pompe Disease
Prader Weely Syndrome
Primary Dystonia
Pseudohypoparathyrosis
Retinitis Pigmentaris
Rett Syndrome
Sandhoff Disease
Sanjad Sakaty
Seckel Disease
Short Chain acyl CoA Dehydrogenase
Skeletal Dysplasia
Smith lemli optiz syndrome
Spina Bifida
Spinal Muscular Atrophy
Thanatophoric Dysplasia
Thrombcytopenia
Tuberous Sclerosis
Very Long Chain acyl CoA Dehydrogenase
Vitamin D Receptors
Wilson disease
X-Linked Deafness
X-linked thrombocytopenia
Y-chromosome Micro Deletion