J Korean Soc Neonatol. Search


Journal of the Korean Society of Neonatology 2008;15(1):89-93.
Published online May 1, 2008.
A Case of Addition of Chromosome 12 associated with Multiple Anomaly and Developmental Impairment.
Yoon Young Chang, Ji Eun Jeong, Jin Young Shin, Hye Jin Park, Kye Hyang Lee, Eun Jin Choi, Jin Kyung Kim, Hai Lee Chung, Eok Su Seo, Woo Taek Kim
1Department of Pediatrics, School of Medicine, Catholic University of Daegu, Daegu, Korea. wootykim@cu.ac.kr
2Department of Opthalmology, College of Medicine, Dongguk University, Gyungju, Korea.
다발성 기형과 발달 장애를 보인 염색체 12번 첨가 1례
, , , , , , , , ,
Duplication of chromosome 12p has been rarely reported and are thought to be associated with congenital malformations and impaired development. We report a baby boy born with multiple dysmorphic features and congenital malformations. His karyotype was 46,XY, add(12)(p13.3). He has suffered from intrauterine growth restriction at birth. He showed abnormal cranio-facial findings such as microcephaly, hypognathia, clepft palate and low set ear. He presented with absence of uvula, micropenis and rocker bottom features of both feet, congenital heart disease, poor corticomedullary differentiation of kidney, and sensorineuronal hearing loss. We have been follow up him for seizure disorder and delayed development at out patient department.
Key Words: Chromosome 12, Addition, Multiple anomaly, Developmental impairmen


Browse all articles >

Editorial Office
34, Sajik-ro 8–gil(King’s Gargen 3 Block 1207), Jongno-gu, Seoul 03174, Republic of Korea
Tel: +82-2-730-1993    Fax: +82-2-730-1994    E-mail: neonate2002@naver.com                

Copyright © 2022 by The Korean Society of Neonatology.

Developed in M2PI

Close layer
prev next