The First Korean Case of De Novo Proximal 4p Deletion Syndrome in a Child With Developmental Delay

Ann Lab Med. 2020 Sep;40(5):435-437. doi: 10.3343/alm.2020.40.5.435.

Authors

Soyoung Park¹, Byung Ryul Jeon², You Kyoung Lee², Chang-Seok Ki³, Mi-Ae Jang²

Affiliations

¹ Department of Pediatrics, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.
² Department of Laboratory Medicine and Genetics, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.
³ GC Genome, Yongin, Korea.

No abstract available

Publication types

Case Reports

MeSH terms

Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 4 / genetics
Developmental Disabilities / diagnosis*
Developmental Disabilities / genetics
Humans
Karyotyping
Male
Republic of Korea
Wolf-Hirschhorn Syndrome / diagnosis*
Wolf-Hirschhorn Syndrome / genetics