Gonosomal mosaicism for an NF1 deletion in a sperm donor: evidence of the need for coordinated, long-term communication of health information among relevant parties

Hum Reprod. 2012 Apr;27(4):1223-6. doi: 10.1093/humrep/des014. Epub 2012 Feb 10.

Abstract

Background: Screening of gamete donors can reduce but cannot eliminate the risks for medical problems in donor-conceived offspring. We present a case of gonosomal mosaicism discovered in an anonymous sperm donor after receiving two reports of neurofibromatosis type 1 (NF1) in donor-conceived offspring, to illustrate that long-term, systematic investigation of health issues in donors and offspring can be invaluable to the welfare of these individuals.

Methods: A repeat physical evaluation and ophthalmology examination were performed on the donor. DNA samples were examined by RTPCR fragment analysis, multiplex ligation-dependent probe amplification (MLPA) and targeted array-comparative genomic hybridization (aCGH).

Results: Gonosomal mosaicism for a deletion mutation in the NF1 gene was identified in 20% of sperm and a smaller percentage of lymphocytes.

Conclusions: Long-term communication of medical information among donors, recipients and donor-conceived offspring is beneficial for the health management of all parties. Development of a secure, coordinated data system is critical to achieving this goal. Recommendations are provided for management and communication of critical information based on this experience.

Publication types

  • Case Reports

MeSH terms

  • California
  • Genetic Counseling
  • Humans
  • Male
  • Medical Records
  • Mosaicism*
  • Neurofibromatosis 1 / genetics*
  • Risk Assessment
  • Sequence Deletion*
  • Spermatozoa*
  • Tissue Donors*