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 |