Literature DB >> 1219125

Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'.

P Jalbert, H Jalbert, B Sele, C Mouriquand, J Malka, J Boucharlat, H Pison.   

Abstract

Five members of a family with a balanced insertion (1;5)(q32;q11q22) are presented. The daughter of one of them shows multiple malformations and a partial trisomy for the long arms of chromosome No. 5 (5q11 to 5q22 segment) resulting from a 'aneusomie de recombinaison' in her mother. The propositus' karyotype is 46,XX,rec(1;5)ins (1;5)(q32;q11q22). This case is the first reported example of an insertion between two chromosomes followed by 'aneusomie de recombinaison'. It also is the first reported case of trisomy invovling the long arms of chromosome No. 5.

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Year:  1975        PMID: 1219125      PMCID: PMC1013326          DOI: 10.1136/jmg.12.4.418

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


  17 in total

1.  [Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].

Authors:  J L Taillemite; G Baheux-Morlier; L Cathelineau; C Roux
Journal:  Ann Genet       Date:  1973-06

2.  Familial insertional translocation.

Authors:  E Grace; G R Sutherland; A D Bain
Journal:  Lancet       Date:  1972-07-29       Impact factor: 79.321

3.  An interstitial translocation: chromosome no. 1p to 4q.

Authors:  J E Gray; J E Syrett; K M Ritchie; W D Elliott
Journal:  Lancet       Date:  1972-07-08       Impact factor: 79.321

4.  [Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)].

Authors:  M O Rethoré; J Lejeune; S Carpentier; M Prieur; B Dutrillaux; P Seringe; A Rossier; J C Job
Journal:  Ann Genet       Date:  1972-09

5.  Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome.

Authors:  K Taysi; M Bobrow; S Balci; K Madan; M Atasu; B Say
Journal:  J Pediatr       Date:  1973-02       Impact factor: 4.406

6.  [Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].

Authors:  B Dutrillaux; C Laurent; J M Robert; J Lejeune
Journal:  Cytogenet Cell Genet       Date:  1973

7.  The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man.

Authors:  M Seabright
Journal:  Chromosoma       Date:  1972       Impact factor: 4.316

8.  Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man.

Authors:  T Caspersson; M Hultén; J Lindsten; L Zech
Journal:  Ann Genet       Date:  1971-06

9.  [On two familial cases of complex translocations].

Authors:  J Lejeune; R Burger
Journal:  Ann Genet       Date:  1965

10.  Aneusomie de recombinaison: three further examples.

Authors:  J de Grouchy; M Aussannaire; H E Brissaud; M Lamy
Journal:  Am J Hum Genet       Date:  1966-09       Impact factor: 11.025

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  13 in total

Review 1.  Intrachromosomal insertions: a case report and a review.

Authors:  K Madan; F H Menko
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

Review 2.  Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Authors:  Joana Barbosa Melo; Liesbeth Backx; Joris R Vermeesch; Heloisa G Santos; Ana C Sousa; Nadezda Kosyakova; Anja Weise; Ferdinand von Eggeling; Thomas Liehr; Isabel Marques Carreira
Journal:  J Appl Genet       Date:  2011-03-25       Impact factor: 3.240

3.  Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7.

Authors:  D R Romain; H Cairney; D Stewart; L M Columbano-Green; M Garry; M I Parslow; R Parfitt; R H Smythe; C J Chapman
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

4.  Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Authors:  M Y Yip; M Selikowitz; N Don; A Kovacic; S Purvis-Smith; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

5.  Clinical manifestations of trisomy 5q.

Authors:  D Kumar; P R Heath; C E Blank
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

6.  Tandem duplication (5q13 to 22) in a mentally deficient girl.

Authors:  E Kessel; R A Pfeiffer
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

Review 7.  Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies.

Authors:  E J Breslau-Siderius; J T Wijnen; J G Dauwerse; J M de Pater; F A Beemer; P M Khan
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

8.  Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5).

Authors:  S Gilgenkrantz; P Dulucq; J L Bresson; A Gouget; C Pernot; M J Gregoire
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

9.  A case of partial 5q trisomy associated with partial 7q monosomy.

Authors:  S Hara; T Yamada; H Nakai; A Ohtani; K Mizuno
Journal:  Br J Ophthalmol       Date:  1986-08       Impact factor: 4.638

10.  Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes.

Authors:  B Zabel; W Baumann; J Gehler; G Conrad
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

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