Literature DB >> 730168

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

K Taysi, G S Sekhon.   

Abstract

Extra chromosome material on the short arm of chromosome no. 6 (46,XY,6p+) was found in two mentally retarded adult half-brothers with mildly dysmorphic features. The phenotypically normal mother had a balanced translocation between the long arm of chromosome no. 1 and the short arm of chromosome no. 6:46,XX,t(1;6)(q32;p25). Thus the two affected brothers were trisomic for the long arm segment of chromosome no. 1, distal to q 32. These patients, with mildly dysmorphic features and mental retardation, represent the first cases of partial trisomy 1q surviving to adult-hood. The clinical and cytogenetic data obtained from eight individuals with partial trisomies for different long arm segments of chromosome no. 1 suggest that partial trisomy of the distal two-thirds of the long arm in characterized by severe malformations, growth retardation, and early death. Conversely, partial trisomy for the distal one-third of the long arm is associated with milder malformations and longer survival time as well as growth and mental retardation.

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Year:  1978        PMID: 730168     DOI: 10.1007/bf00394292

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  8 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 of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.

Authors:  D M Steffensen; E H Chu; D P Speert; P M Wall; K Meilinger; R P Kelch
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

3.  Trisomy of the long arm of human chromosome 1.

Authors:  T H Norwood; H Hoehn
Journal:  Humangenetik       Date:  1974

4.  The relationship between patterns of DNA replication and of quinacrine fluorescence in the human chromosome complement.

Authors:  E Ganner; H J Evans
Journal:  Chromosoma       Date:  1971       Impact factor: 4.316

5.  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

6.  Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes.

Authors:  M Holmberg; J Jonasson
Journal:  Hereditas       Date:  1973       Impact factor: 3.271

7.  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

8.  "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

  8 in total
  8 in total

1.  Partial 1q and 21p trisomies in a male child due to maternal t(1;21).

Authors:  S Rajangam; S Lincoln; S Hegde; I M Thomas
Journal:  Indian J Pediatr       Date:  1999 Mar-Apr       Impact factor: 1.967

2.  Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.

Authors:  H C Duba; M Erdel; J Löffler; L Bereuther; H Fischer; B Utermann; G Utermann
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

3.  Omphalocele and partial trisomy 1q syndrome.

Authors:  H Chen; J J Gershanik; J B Mailhes; I D Sanusi
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

4.  Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1).

Authors:  A E Vauhkonen; E M Sankila; K O Simola; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

5.  Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

6.  Partial trisomy 1 due to 1/17 translocation in Ph'-positive chronic myelocytic leukemia.

Authors:  F Pasquali; D Francesconi; R Casalone; G Ippoliti
Journal:  Hum Genet       Date:  1979-07-18       Impact factor: 4.132

7.  Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome.

Authors:  G Pierquin; N Van Regemorter; C Fourneau; J Bormans; M Foerster; E Damis; N Cremer-Perlmutter; C M Lapiere; E Vamos
Journal:  Hum Genet       Date:  1991-09       Impact factor: 4.132

8.  18q+, the progeny of a balanced translocation t(1;18)mat: case report with necropsy findings.

Authors:  A Hindi; D Beneck; M A Greco; S R Wolman
Journal:  J Med Genet       Date:  1986-06       Impact factor: 6.318

  8 in total

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