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First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p

Crossref DOI link: https://doi.org/10.1186/s43042-024-00619-x

Published Online: 2024-12-30

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Satekge, Tumelo M. https://orcid.org/0000-0002-0930-249X
Rikhotso, Glenrose

Rossouw, Bianca

Dillon, Bronwyn

Baine-Savanhu, Fiona
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Text and Data Mining valid from 2024-12-30

Version of Record valid from 2024-12-30
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Article History

Received: 25 June 2024

Accepted: 5 December 2024

First Online: 30 December 2024

Declarations

:

: Ethics clearance was obtained from the Polokwane Mankweng Research Ethics Committee (PMREC) (REC 300408-006).

: All consent for publications was taken before submission of manuscript.

: The authors declare that there are no competing interests regarding the publication of this article.

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