You are here

  • Home
  • Archive
  • Volume 15, Issue 5
  • Late maternal diagnosis of DiGeorge syndrome with congenital hypoparathyroidism following antenatal detection of the same 22q11.2 microdeletion syndrome in the fetus

Article info

Article menu
Download PDFPDF
Case Reports: Reminder of important clinical lesson
Late maternal diagnosis of DiGeorge syndrome with congenital hypoparathyroidism following antenatal detection of the same 22q11.2 microdeletion syndrome in the fetus

Authors

  1. Correspondence to Dr Alexandros Leonidas Liarakos; alexandros.liarakos{at}gmail.com
View Full Text

Citation

Liarakos AL, Tran P, Rao R, et al
Late maternal diagnosis of DiGeorge syndrome with congenital hypoparathyroidism following antenatal detection of the same 22q11.2 microdeletion syndrome in the fetus
BMJ Case Reports CP 2022;15:e250350.

Publication history

  • Accepted May 8, 2022
  • First published May 20, 2022.
Online issue publication 
January 24, 2024

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Copyright information

© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.