Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Liena Elbaghir Omer Elsayed¹, Norah Ayed AlHarbi², Ashwaq Mohammed Alqarni³, Huda Hussein Elwasila Eltayeb¹, Noura Mostafa Mohamed Mostafa^{1

4}, Maha Mohammed Abdulrahim⁵, Hadeel Ibrahim Bin Zaid⁶, Latifah Mansour Alanzi⁷, Sarah Abdullah Ababtain⁸, Khawlah Aldulaijan⁸, Sheka Yagub Aloyouni⁸, Moneeb Abdullah Kassem Othman⁹, Mohammad Abdullah Alkheilewi¹⁰, Adel Mohammed Binduraihem⁸, Hadeel Abdollah Alrukban¹¹, Hiba Yousif Ahmed¹², Faten Abdullah AlRadini¹³, Hadil Mohammad Alahdal¹⁴, Aziza Mufareh Mushiba^{12

15}, Omaima Abdulazeem Alzaher¹⁶

Affiliations

¹ Department of Basic Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
² Department of Internal Medicine, College of Medicine, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia. Noaalharbi@pnu.edu.sa.
³ Foundation Year of Health Colleges, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁴ Medical Biochemistry Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
⁵ Research and Academic Accreditation, Academic Affairs, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
⁶ Out-Patient department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁷ Department of Pathology and Laboratory Medicine, King Abdullah Bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁸ Genetics Section, Research Department, Health Sciences Research Center, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
⁹ Centogene GmbH, Rostock, Germany.
¹⁰ Health Support Services Centre, Ministry of Health, Riyadh, 12382, Saudi Arabia.
¹¹ Pediatric Department, Division of Genetic and Metabolic, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
¹² Pediatrics department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
¹³ Family and Community Medicine Department, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
¹⁴ Department of Biology, College of Science, Princes Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
¹⁵ Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
¹⁶ Pediatric Department, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.

PMID: 39407347
PMCID: PMC11475645
DOI: 10.1186/s40246-024-00681-x

Published Erratum

Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Liena Elbaghir Omer Elsayed et al. Hum Genomics. 2024.

. 2024 Oct 15;18(1):115.

doi: 10.1186/s40246-024-00681-x.

Authors

Affiliations

¹ Department of Basic Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
² Department of Internal Medicine, College of Medicine, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia. Noaalharbi@pnu.edu.sa.
³ Foundation Year of Health Colleges, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁴ Medical Biochemistry Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
⁵ Research and Academic Accreditation, Academic Affairs, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
⁶ Out-Patient department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁷ Department of Pathology and Laboratory Medicine, King Abdullah Bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
⁸ Genetics Section, Research Department, Health Sciences Research Center, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
⁹ Centogene GmbH, Rostock, Germany.
¹⁰ Health Support Services Centre, Ministry of Health, Riyadh, 12382, Saudi Arabia.
¹¹ Pediatric Department, Division of Genetic and Metabolic, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
¹² Pediatrics department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
¹³ Family and Community Medicine Department, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
¹⁴ Department of Biology, College of Science, Princes Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
¹⁵ Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
¹⁶ Pediatric Department, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.

PMID: 39407347
PMCID: PMC11475645
DOI: 10.1186/s40246-024-00681-x

No abstract available

PubMed Disclaimer

Erratum for

Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Elsayed LEO, AlHarbi NA, Alqarni AM, Eltayeb HHE, Mostafa NMM, Abdulrahim MM, Zaid HIB, Alanzi LM, Ababtain SA, Aldulaijan K, Aloyouni SY, Othman MAK, Alkheilewi MA, Binduraihem AM, Alrukban HA, Ahmed HY, AlRadini FA, Alahdal HM, Mushiba AM, Alzaher OA. Elsayed LEO, et al. Hum Genomics. 2024 Sep 4;18(1):95. doi: 10.1186/s40246-024-00662-0. Hum Genomics. 2024. PMID: 39232803 Free PMC article.

Publication types

Actions

LinkOut - more resources

Full Text Sources
- BioMed Central
- PubMed Central

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Affiliations

Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Authors

Affiliations

Erratum for

Publication types

LinkOut - more resources

Full Text Sources