Korean J Perinatol.  2010 Dec;21(4):403-407.

A Case of Partial Trisomy 14q derived from Paternal Balanced Translocation

Affiliations
  • 1Department of Pediatrics, Presbyterian Medical Center, Jeonju, Korea. okleepmc@naver.com
  • 2Department of Laboratory Medicine, Presbyterian Medical Center, Jeonju, Korea.

Abstract

Partial trisomy 14q is an extremely rare disorder. Approximately 50 cases have been reported around the world. This disorder results from a malsegregation or non-disjunction of balanced translocated chromosome, thus the offspring inherits such a chromosome. In this report, the father's chromosomal arrangement was 46, XY, t(11;14)(q25;q32.1) and the mother had a normal chromosomal arrangement. We experienced a case of partial trisomy 14q in a male neonate who had craniofacial abnormalities, frontal bossing, bulgin fontanelle, hypertelorism, low-set ears, wide and flat nasal bridge, thin cupid bow lip and micrognathia. The karyotype of his chromosome was 46,XY,der(11)t(11;14)(q25;q32.1). We report the case with a review of the literature.

Keyword

Trisomy; Chromosome 14q; Balanced translocation

MeSH Terms

Craniofacial Abnormalities
Ear
Humans
Hypertelorism
Infant, Newborn
Karyotype
Lip
Male
Mothers
Trisomy
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