Single Gene Disorder PGD

Argenomics carries the unique distinction of testing single gene disorders on embryos for the first time in India. Over the course of our journey so far, we have dealt with a large number of autosomal recessive, autosomal dominant as well as X linked disorders.

The genetic abnormality, single gene disorder happens when either both the parents are carriers of a faulty gene or one of the parent is a carrier who in turn pass the gene to his/her offspring. Genetic diseases vary as per their modes of inheritance. Argenomics can help prevent the condition passing on to children irrespective of the inheritance mode.

Examples of these relatively common single gene disorders include:

• Thalassemia
• Sickle Cell Anaemia
• Hemophilia
• Spinal Muscular Atrophy
• Inborn errors of metabolism

Some of our PGD SGD achievements

• Tay sachs
• Thalassemia
• Hemophilia
• Smn1