Single Gene Disorders

PGD can be performed for nearly all single gene disorders, as long as the specific genetic mutation is known. This includes (but is not limited to):
 
Beta-Thalassemia
Cystic Fibrosis (CF)
Duchenne Muscular Dystrophy (DMD)
Dystonia (Type 1)
Facioscapulohumeral Muscular Dystrophy (FSHD)
Fragile X Syndrome
Hemophilia Type A
Hereditary Breast/Ovarian Cancer (BRCA1 and BRCA2)
HLA matching
Huntington’s Disease (HD)
Myotonic Dytrophy (DM)
Sickle Cell Anemia
Spinal Muscular Atrophy (SMA)
 

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