Literature DB >> 7218339

Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities.

M Zannotti, A Preto, P R Giovanardi, B Dallapiccola.   

Abstract

Five unrelated patients with a supernumerary chromosome derivative of chromosome 15 are described. The clinical findings in the present series of cases show a gross concordance with the data previously reported in subjects with similar aberrations and allow the delineation of a distinct syndrome. Although undetermined variation in the structure of these extra chromosomes may contribute significantly to phenotypic heterogeneity, the patients display a rather common constellation of findings, which include: absence of major malformations, mental and developmental retardation, seizures, hypotonia, behavioural disturbances, and reduced total ridge count on fingertips. Patients with partial trisomy 15q- resulting from dicentric chromosomes bear little resemblance to patients carrying 15q- chromosomes arising de novo or due to unbalanced translocations.

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Year:  1980        PMID: 7218339     DOI: 10.1111/j.1365-2788.1980.tb00077.x

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN: 0022-264X


  8 in total

1.  Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

Authors:  R Plattner; N A Heerema; S R Patil; P N Howard-Peebles; C G Palmer
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

Review 2.  Inv dup(15) supernumerary marker chromosomes.

Authors:  T Webb
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

3.  Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.

Authors:  R Plattner; N A Heerema; P N Howard-Peebles; J H Miles; S Soukup; C G Palmer
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

4.  An analysis of the parental age effect for inv dup (15).

Authors:  J M Connor; D H Gilmore
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

5.  Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

Authors:  A E Wandstrat; J Leana-Cox; L Jenkins; S Schwartz
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

Review 6.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Inv dup (15) with mental retardation but few dysmorphic features.

Authors:  D H Gilmore; E Boyd; J P McClure; P Batstone; J M Connor
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

8.  Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder.

Authors:  Yinghong Lu; Yi Liang; Sisi Ning; Guosheng Deng; Yuling Xie; Jujie Song; Na Zuo; Chunfeng Feng; Yunrong Qin
Journal:  Mol Cytogenet       Date:  2020-06-10       Impact factor: 2.009

  8 in total

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