Literature DB >> 1753439

Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).

T Asano1, T Ikeuchi, T Shinohara, H Enokido, K Hashimoto.   

Abstract

A 7-year-old boy with dysmorphic features was found to have a recombinant chromosome 18, rec(18), resulting from meiotic recombination of a maternal pericentric inversion, inv(18) (p11.2q21.3), as defined by high-resolution banding. He was trisomic for the long arm (q21.3-qter) and monosomic for the short arm (p11.2-pter) of chromosome 18. His clinical features were compared with those in other rec(18) cases, and also those in monosomy 18p, trisomy 18qter and full trisomy 18 syndromes. The risk of recombinant formation for inv(18) carriers was also discussed.

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Year:  1991        PMID: 1753439     DOI: 10.1007/BF01910544

Source DB:  PubMed          Journal:  Jinrui Idengaku Zasshi        ISSN: 0021-5074


  3 in total

Review 1.  Partial trisomy 18q.

Authors:  M Elbistan; S Kucukoduk; N Kara
Journal:  Indian J Pediatr       Date:  1996 May-Jun       Impact factor: 1.967

2.  A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria.

Authors:  Julio A Poterico; Flor Vásquez; Miguel Chávez-Pastor; Milana Trubnykova; Félix Chavesta; Jenny Chirinos; Nancy Salcedo; Rosmery Mena; Sulema Cubas; Rocío González; Rossana Alvariño; Hugo Abarca-Barriga
Journal:  J Pediatr Genet       Date:  2017-07-06

3.  Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Authors:  Ariana Kariminejad; Roxana Kariminejad; Azadeh Moshtagh; Maryam Zanganeh; Mohammad Hassan Kariminejad; Stefan Neuenschwander; Michal Okoniewski; Eva Wey; Albert Schinzel; Alessandra Baumer
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246

  3 in total

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