Clinical and Experimental Pediatrics

대한소아청소년과학회 (The Korean Pediatric Society)
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A chromosome 1q44 deletion in a 4-month-old girl; The first report in Korea

  • Cho, Joo Hyun (Department of Pediatrics, Chonnam National University Hospital) ;
  • Song, Eun Song (Department of Pediatrics, Chonnam National University Hospital) ;
  • Kim, Hee Na (Department of Pediatrics, Chonnam National University Hospital) ;
  • Oh, Burm Seok (Department of Pediatrics, Chonnam National University Hospital) ;
  • Choi, Young Youn (Department of Pediatrics, Chonnam National University Hospital)
  • 투고 : 2013.05.07
  • 심사 : 2013.10.07
  • 발행 : 2014.06.10
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초록

The deletion of the distal long arm of chromosome 1 is associated with a characteristic facial appearance and a pattern of associated malformations. Characteristic manifestations include a round face with prominent 'cupid's bow' and downturned corners of the mouth, thin vermilion borders of lips, a long upper lip with a smooth philtrum, a short and broad nose, epicanthal folds, apparently low-set ears, micrognathia, microcephaly, abnormal hands and feet, variable cardiac or genital anomalies, moderate to severe mental retardation, and growth retardation. Using fluorescent in situ hybridization (FISH) analysis to map precisely the deletion, we present a case of chromosome 1q44 deletion with craniofacial characteristics, multiple congenital anomalies, and growth and psychomotor retardation. In comparison with other reported cases of 1q43-44 deletion, the subject does not show hydrocephalus, seizure, syn- or polydactyly of hands, and a urogenital anomaly. However, an arachnoid cyst, pinpoint dimple on the midline of the forehead, a right-sided supernumerary nipple and auricular pit, polydactyly of the right foot, adducted thumb, and flexion restriction of the proximal interphalangeal joint with a simian line in both hands were observed additionally.

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참고문헌

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피인용 문헌

  1. A Case of Chromosome 1q44 Deletion with Microcephaly and Multiple Congenital Anomalies vol.25, pp.2, 2014, https://doi.org/10.14734/kjp.2014.25.2.95
  2. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer–Rokitansky–Küster vol.30, pp.7, 2015, https://doi.org/10.1093/humrep/dev095
  3. Analysis copy number variation of Chinese children in early‐onset epileptic encephalopathies with unknown cause vol.90, pp.5, 2014, https://doi.org/10.1111/cge.12768
  4. Chromosome microarray analysis in the investigation of children with congenital heart disease vol.17, pp.1, 2014, https://doi.org/10.1186/s12887-017-0863-3
  5. Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation vol.11, pp.None, 2014, https://doi.org/10.1186/s13039-018-0406-0
  6. Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobands vol.13, pp.3, 2014, https://doi.org/10.1136/bcr-2019-231938