Literature DB >> 18568304

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.

Gopalrao V N Velagaleti1, Judy C Hawkins, Neli I Panova, Lillian H Lockhart.   

Abstract

Partial trisomy 7p with partial monosomy 9p is a rare disorder with only 3 cases reported. Both these abnormalities i.e., partial trisomy 7p and partial monosomy 9p result in distinct clinical phenotypes. However, patients with combined 7p trisomy/9p monosomy present with a phenotype consistent with trisomy 7p. We present a fourth case of trisomy 7p/monosomy 9p with long term follow-up and document the medical complications associated with this disorder. Long term follow-up of patients with chromosome abnormalities provides a unique opportunity to document the medical history and complications associated with such abnormalities.

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Year:  2008        PMID: 18568304     DOI: 10.1007/s12098-008-0093-7

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  30 in total

1.  Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Authors:  L A Christ; C A Crowe; M A Micale; J M Conroy; S Schwartz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

3.  Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses.

Authors:  F Vialard; C Ottolenghi; M Gonzales; A Choiset; S Girard; J P Siffroi; K McElreavey; C Vibert-Guigue; M Sebaoun; N Joyé; M F Portnoï; F Jaubert; M Fellous
Journal:  J Med Genet       Date:  2002-07       Impact factor: 6.318

4.  [Partial 7p trisomy. Report of new phenotype features].

Authors:  E Román Ortiz; M López-Sánchez-Solís de Querol; M D Peris-Mencheta Ríos-Melida; M Pajarón de Ahumada; M Gracian Gómez; J M Guia Torrent; R Fernández Parra; I Martínez-Artero Martínez; J Gabarrón; F Salvat Germán
Journal:  An Esp Pediatr       Date:  1992-01

Review 5.  Jumping translocation with partial duplications and triplications of chromosomes 7 and 15.

Authors:  T Jewett; D Marnane; W Stewart; R Hayworth-Hodge; L Finklea; K Klinepeter; P N Rao; M J Pettenati
Journal:  Clin Genet       Date:  1998-05       Impact factor: 4.438

Review 6.  De novo duplication of 7pter-->p21.2 and deletion of 9pter-->p23.5: clinical and cytogenetic diagnosis.

Authors:  E Back; C Jung; S Zeitler; W Schempp
Journal:  Clin Genet       Date:  1997-01       Impact factor: 4.438

7.  Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotype.

Authors:  J Gabarrón; G Glover; A Jiménez; P Salas; J Pérez-Bryan; M J Parra
Journal:  Clin Genet       Date:  1988-03       Impact factor: 4.438

8.  Mutations of the TWIST gene in the Saethre-Chotzen syndrome.

Authors:  V el Ghouzzi; M Le Merrer; F Perrin-Schmitt; E Lajeunie; P Benit; D Renier; P Bourgeois; A L Bolcato-Bellemin; A Munnich; J Bonaventure
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

9.  Mutation of HOXA13 in hand-foot-genital syndrome.

Authors:  D P Mortlock; J W Innis
Journal:  Nat Genet       Date:  1997-02       Impact factor: 38.330

10.  Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.

Authors:  K Ounap; O Uibo; R Zordania; L Kiho; T Ilus; E Oiglane-Shlik; O Bartsch
Journal:  Am J Med Genet A       Date:  2004-11-01       Impact factor: 2.802

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