First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)

• Published in: Prenatal diagnosis 2002-06, Vol.22 (6), p.519-524
• Main Authors: Abou-Sleiman, P. M., Apessos, A., Harper, J. C., Serhal, P., Winston, R. M. L., Delhanty, J. D. A.
• Format: Article
• Language: English
• Subjects: Adult; Biopsy; Blastomeres; DNA Mutational Analysis; Embryo Transfer; Fertilization in Vitro; fluorescent SSCP; Genes, Neurofibromatosis 2; Humans; Male; Mutation; Neurofibromatosis 2 - diagnosis; Neurofibromatosis 2 - genetics; neurofibromatosis type 2; NF2; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Preimplantation Diagnosis; preimplantation genetic diagnosis (PGD); Sequence Analysis, DNA; single cell PCR
• ISSN: 0197-3851; 1097-0223
• DOI: 10.1002/pd.393

Neurofibromatosis type 2 (NF2) is a dominantly inherited cancer predisposition syndrome that is caused bymutations in the NF2 gene. We report here the first clinical preimplantation genetic diagnosis (PGD) forNF2. A protocol was developed to simultaneously amplify the mutation and a single nucleotide polymorphism (SNP) located within the gene. The mutation and polymorphism were analysed by simultaneous fluorescent single‐strand conformation polymorphism (SSCP) on an automated DNA sequencer. The mutation, carried by the male partner, was a single base pair substitution affecting a splice site in intron 4 of the gene. The female partner was infertile due to polycystic ovary syndrome and would require IVF to conceive. The couple was found to be informative at a linked intragenic SNP situated in the 5′ untranslated region of the gene. The SNP was included in the assay to reduce the risk of misdiagnosis due to allele dropout (ADO). The couple underwent three cycles of treatment during which a total of 43 blastomeres were biopsied from 31 embryos. Amplification at both loci was obtained in 35 cells (81%). A total of five embryos were transferred, two in the first cycle, two in the second and one in the third. No pregnancy ensued. The results of the diagnoses indicated that, in this couple, the inheritance of the mutation may be non‐Mendelian. Out of a total of 32 embryos tested only four were found not to carry the mutation. The reasons for this apparent skew remain unknown. Copyright © 2002 John Wiley & Sons, Ltd.