A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome

Clin Dysmorphol. 2021 Oct 1;30(4):181-185. doi: 10.1097/MCD.0000000000000380.

Authors

Hagit Goldenstein¹, Sara Beni Shrem², Omri Weiss³, Sharon Zeligson³, Reeval Segel³, Adi Mory⁴, Karin Weiss^{1

4}

Affiliations

¹ The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa.
² Pediatric Neurodevelopment Service, Meuchedet Health Services.
³ Medical Genetics Institute, Shaare Zedek Medical Center and Hebrew University-Hadassah School of Medicine, Jerusalem.
⁴ The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.

PMID: 34232135
DOI: 10.1097/MCD.0000000000000380

No abstract available

MeSH terms

Child
Chromosome Aberrations*
Chromosome Deletion*
Chromosomes, Human, Pair 5 / genetics
Humans
Syndrome