Literature DB >> 3723558

18q+, the progeny of a balanced translocation t(1;18)mat: case report with necropsy findings.

A Hindi, D Beneck, M A Greco, S R Wolman.   

Abstract

A female infant with additional genetic material on the long arm of chromosome 18 is described. Cytogenetic studies of the infant and her mother showed that the altered region resulted from an unbalanced translocation of part of the long arm of chromosome 1. This chromosomal abnormality has not been reported previously, according to a recent registry of abnormal chromosome patterns. The patient had hydrops fetalis and multiple congenital abnormalities, involving the cardiovascular, respiratory, and skeletal systems, together with unusual facies. External features, radiological findings, and gross and microscopical examination at necropsy are presented and compared with previously reported cases of related but dissimilar chromosomal abnormalities.

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Year:  1986        PMID: 3723558      PMCID: PMC1049641          DOI: 10.1136/jmg.23.3.263

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  9 in total

1.  Fetal loss and familial chromosome 1 translocations.

Authors:  J H Garrett; S C Finley; W H Finley
Journal:  Clin Genet       Date:  1975-11       Impact factor: 4.438

2.  Partial trisomy 1q syndrome.

Authors:  H Rehder; U Friedrich
Journal:  Clin Genet       Date:  1979-06       Impact factor: 4.438

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

4.  Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Authors:  H Van den Berghe; M Van Eygen; J P Fryns; W Tanghe; H Verresen
Journal:  Humangenetik       Date:  1973-05-25

5.  A partial trisomy of chromosome 1 in a family with a t(1q-;4q+) translocation.

Authors:  R L Neu; L I Gardner
Journal:  Clin Genet       Date:  1973-06       Impact factor: 4.438

6.  "De novo" trisomy 1q32 leads to 1qter and monosomy 3p25 leads to 3pter.

Authors:  E Yunis; H Egel; R Zúñiga; E Ramirez; O M Torres de Caballero; M Leibovici
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

7.  Partial trisomy of the long arm of chromosome 1 due to a familial translocation t(1;10) (q32;q26).

Authors:  A Bonfante; M Stella; G Rossi
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

8.  Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).

Authors:  K Taysi; G S Sekhon
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

9.  Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].

Authors:  M G Wilson; J W Towner; I Forsman; E Siris
Journal:  Am J Med Genet       Date:  1979
  9 in total
  1 in total

1.  The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Authors:  G A Silverman; S S Schneider; H F Massa; A Flint; M Lalande; J C Leonard; J Overhauser; G van den Engh; B J Trask
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

  1 in total

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