Literature DB >> 15470365

Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.

Stefan J Vermeulen1, Frank Speleman, Leen Vanransbeeck, Jasmien Verspeet, Björn Menten, Marie-Rose Verschraegen-Spae, Philippe De Wilde, Ludwine Messiaen, Ron C Michaelis, Jules G Leroy.   

Abstract

We describe a family in which the largest hitherto reported pericentric inversion of chromosome 18, inv(18)(p11.22q23), segregates. Individuals heterozygous for the nonrecombinant inversion were unaffected. However, those heterozygous for either the dup(18p)/del(18q) or dup(18q) /del(18p) recombinant exhibited mild learning difficulty, personality disorders and deficient social behavior in the absence of mental retardation. Of the three family members tested, the behavioral abnormalities were more prominent in the two individuals with the dup(18p)/del(18q) recombinant than in the one with the dup(18q)/del(18p) recombinant. Genetic counseling issues for this family, in particular for the affected, include the enhanced probability of reduced fertility as well as the recurrence risk of the parental inversion equaling 1/2 in surviving offspring. This observation kindles the interest in determining the frequency of subtelomeric rearrangements in individuals with learning difficulty and deficiency in social interaction, phenotypic features often considered to be of multifactorial causation.

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Year:  2005        PMID: 15470365     DOI: 10.1038/sj.ejhg.5201281

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  3 in total

1.  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

2.  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.  Chromosome 18p11.2 harbors susceptibility marker: D18S452, for bipolar affective disorder.

Authors:  Mutahar Andrabi; Arshad Hussain; Fouzia Rashid; Sheikh Ozair Nissar; Idrees Ayoub Shah; Yasir Hasan Rather; Waseem Hassan Ahangar; Nazir Ahmad Dar
Journal:  Indian J Psychiatry       Date:  2013-10       Impact factor: 1.759

  3 in total

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