Evidence map›Paper›PMID 39414661›Full record

ReviewPediatric nephrology (Berlin, Germany)2025

Diagnosing a genetic disease in a donor-conceived child: case report and discussion of the ethical, legal, and practical issues.

Mathieu Lemaire, Damien Noone, Larissa Waldman, Kimberly E Liu, Jaap Mulder, Sara R Cohen, Rebecca A Greenberg, Lauren Chad

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mathieu LemaireDivision of Nephrology, The Hospital for Sick Children, Toronto, Ontario, Canada. mathieu.lemaire@sickkids.ca.ORCID http://orcid.org/0000-0001-7593-6418
Damien NooneDivision of Nephrology, Stollery Children's Hospital, Edmonton, University of Alberta, Edmonton, Canada.
Larissa WaldmanCancer Genetics and High-Risk Program, Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada.
Kimberly E LiuDepartment of Obstetrics and Gynecology, University of Toronto, Toronto, ON, Canada.
Jaap MulderDivision of Nephrology, Department of Pediatrics, Erasmus MC, Rotterdam, the Netherlands.
Sara R CohenFertility Law Canada at D2Law LLP, Toronto, Ontario, Canada.
Rebecca A GreenbergDepartment of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
Lauren ChadDepartment of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada. lauren.chad@sickkids.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe the unexpected challenges pediatricians may experience when children conceived with assisted reproduction are diagnosed with a rare genetic condition. A local case series triggered a dialogue between many stakeholders with varied expertise. Indeed, diagnosing a genetic disease in a child conceived by embryo, egg, or sperm donation is becoming more common now that genetic testing and in vitro fertilization (IVF) are readily accessible. However, how and whether to share that information with other stakeholders in the gamete donation process has not been fully explored, and the clinical responsibilities of the treating clinician remain ill-defined. This work centers on a patient with a confirmed diagnosis of X-linked nephrogenic diabetes insipidus. Ultimately, we found the same AVPR2 mutation in two children from two families conceived by egg donation. It led to multigenerational cascade diagnoses in the family of the shared, anonymous egg donor. First, we review current genetic testing practices in gamete donation and third-party reproduction. Then, we provide an overview of relevant genomic, ethical, legal, and psychosocial considerations for sharing relevant genomic information. Finally, and to maximize the best interests of genetic relatives, we discuss how a pediatrician can play a role in the early disclosure of relevant clinical information to all stakeholders in the gamete donation process, starting with the fertility clinic. While these clinical cases are cast in a Canadian context, we submit that its important lessons generally apply to medical systems of nearly all developed countries, broadly defined.

Indexed as

Genetic Diseases, X-LinkedGenetic TestingOocyte DonationChildFemaleHumansMaleTissue DonorsAVRP2Donor-conceived childrenFertility clinicGamete donorIn vitro fertilizationNephrogenic diabetes insipidusRare genetic disease

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.