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Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report

Crossref DOI link: https://doi.org/10.1186/s12887-018-1161-4

Published Online: 2018-06-04

Published Print: 2018-12

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

Authors

Berrani, H. http://orcid.org/0000-0001-9687-6389
Meskini, T.

Zerkaoui, M.

Merhni, H.

Ettair, S.

Sefiani, A.

Mouane, N.
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Article History

Received: 11 January 2018

Accepted: 29 May 2018

First Online: 4 June 2018

Ethics approval and consent to participate

: Written informed consent was obtained from the parents of the patient for the genetic analysis and publication of any accompanying images of this case report. This study was approved by the Human Research Ethic Committee at the Faculty of Medicine of Rabat, Mohammed V University, Morocco.

: Written informed consent was obtained from the patient’s parents for publication of this case report and any accompanying images.

: The authors declare that they have no competing interests.

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