Repeated transmission of X-linked ocular albinism type 1 by a carrier oocyte donor

Fertil Steril. 1998 Dec;70(6):1169-72. doi: 10.1016/s0015-0282(98)00387-2.

Abstract

Objective: To report the transmission of unsuspected X-linked ocular albinism in an oocyte donor program.

Design: Case report.

Setting: University medical center.

Patient(s): A 24-year-old white female oocyte donor and the outcomes of three recipient pregnancies.

Intervention(s): Clinical assessment and molecular diagnostic tests.

Main outcome measure(s): Mutation detection.

Result(s): Demonstration of carrier status and multiple transmissions of a mutant allele.

Conclusion(s): We describe the transmission of a mutant allele for X-linked ocular albinism from an unsuspected carrier female oocyte donor to three independent pregnancies. We emphasize the need for diligent inquisition to clarify any unusual history of ocular or constitutional signs that might signify an X-linked disorder.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Albinism, Ocular / genetics*
  • Female
  • Genetic Carrier Screening*
  • Genetic Linkage*
  • Humans
  • Pregnancy
  • Pregnancy Outcome
  • Tissue Donors*
  • X Chromosome*