Literature DB >> 8116670

An infant with double trisomy (48,XXX, + 18)

S Jaruratanasirikul1, U Jinorose.   

Abstract

We report on an infant with double trisomy 48,XXX, + 18. She presented with manifestations of trisomy 18: prominent occiput, microphthalmia, small mouth, micrognathia, malformed ears, congenital heart defect, overlapping fingers, talipes equinovarus, and rockerbottom feet. An extra palmar crease was present only on the right hand. This patient was alive at 12 months. The clinical manifestations are compared with those of 10 previously reported cases.

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Year:  1994        PMID: 8116670     DOI: 10.1002/ajmg.1320490210

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Double trisomy 48,XXX,+18 with multiple dysmorphic features.

Authors:  Zi-Yan Jiang; Xiao-Hui Wu; Chao-Chun Zou
Journal:  World J Pediatr       Date:  2015-01-28       Impact factor: 2.764

2.  Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.

Authors:  V M Park; R R Bravo; L P Shulman
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

3.  Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients.

Authors:  Osman Demirhan; Erdal Tunç
Journal:  Chromosoma       Date:  2022-10-11       Impact factor: 2.919

4.  Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18.

Authors:  Sujal I Shah; Lisa Dyer; Jerzy Stanek
Journal:  Case Rep Pathol       Date:  2018-03-08
  4 in total

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