A case series of adrenoleukodystrophy in children conceived through in vitro fertilization with an egg donor.

ALD Adrenoleukodystrophy case report genetic testing in vitro fertilization

Journal

F&S reports
ISSN: 2666-3341
Titre abrégé: F S Rep
Pays: United States
ID NLM: 101766618

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 03 08 2022
revised: 15 11 2022
accepted: 16 12 2022
entrez: 24 3 2023
pubmed: 25 3 2023
medline: 25 3 2023
Statut: epublish

Résumé

To report 3 cases of adrenoleukodystrophy (ALD) in children conceived by in vitro fertilization (IVF) and egg donation. A case report. Patients aged 4-5 years old, evaluated by the University of Minnesota Leukodystrophy Center, who were diagnosed with ALD after being conceived by IVF with oocytes provided by the same donor. One patient received a hematopoietic stem cell transplant from a human leukocyte antigen-matched donor, and 1 patient received autologous lentiviral corrected hematopoietic cells. The disease state in 1 patient was unfortunately too advanced for effective treatment to be administered. Progression of disease after diagnosis or treatment was observed by cerebral magnetic resonance imaging and monitoring the development or advancement of any cognitive, adaptive, and motor deficits. Patients who received a transplant for ALD successfully experienced little to no disease progression at least 6 months to 1 year after treatment. These 3 cases of transmission of ALD through oocyte donation and IVF highlight the potential need to implement more comprehensive genetic screening of gamete donors to prevent the transfer of rare but severe genetic diseases through IVF. Further, these cases highlight limitations in carrier screening guidelines that limit reportable variants to pathogenic and likely pathogenic variants.

Identifiants

pubmed: 36959964
doi: 10.1016/j.xfre.2022.12.005
pii: S2666-3341(22)00142-8
pmc: PMC10028476
doi:

Types de publication

Journal Article

Langues

eng

Pagination

24-28

Informations de copyright

© 2022 The Author(s).

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Auteurs

Crystal Chang (C)

Division of Pediatric Blood and Marrow Transplantation and Cellular Therapy Program, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.

Ashish O Gupta (AO)

Division of Pediatric Blood and Marrow Transplantation and Cellular Therapy Program, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.

Paul J Orchard (PJ)

Division of Pediatric Blood and Marrow Transplantation and Cellular Therapy Program, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.

David R Nascene (DR)

Department of Radiology, University of Minnesota Medical School, Minneapolis, Minnesota.

Janell Kierstein (J)

Department of Genetics and Metabolism, Children's Hospital Colorado, Aurora, Colorado.

Rebecca K Tryon (RK)

Division of Pediatric Blood and Marrow Transplantation and Cellular Therapy Program, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
Department of Genetics, M Health Fairview, Minneapolis, Minnesota.

Troy C Lund (TC)

Division of Pediatric Blood and Marrow Transplantation and Cellular Therapy Program, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.

Classifications MeSH