A Case of Addition of Chromosome 12 associated with Multiple Anomaly and Developmental Impairment.
- Author:
Yoon Young CHANG
1
;
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
Author Information
1. Department of Pediatrics, School of Medicine, Catholic University of Daegu, Daegu, Korea. wootykim@cu.ac.kr
- Publication Type:Case Report
- Keywords:
Chromosome 12;
Addition;
Multiple anomaly;
Developmental impairmen
- MeSH:
Chromosomes, Human, Pair 12;
Ear;
Epilepsy;
Follow-Up Studies;
Foot;
Genital Diseases, Male;
Hearing Loss;
Heart Diseases;
Humans;
Karyotype;
Kidney;
Microcephaly;
Palate;
Parturition;
Penis;
Uvula
- From:Journal of the Korean Society of Neonatology
2008;15(1):89-93
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
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.
