Literature DB >> 2722199

Partial trisomy of distal 8q derived from mother with mosaic 8q23.3----24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I.

K Naritomi1, K Hirayama.   

Abstract

A 17-month-old girl with a partial trisomy of distal 8q derived from her mother, who has a mosaic 8q23.3----q24.13 deletion, was studied. Both showed a relatively mild phenotype of trichorhinophalangeal syndrome I. The karyotype of the proposita was designated as: 46,XX,-8,+der(8),inv ins(8;8)(p23.1;q24.13q23.3)mat. Her phenotype was considered similar to that of her mother despite the trisomies of distal 8q. She seems to be the first example of a partial trisomy of distal 8q derived from a parent with an interstitial deletion of a distal 8q segment and trichorhinophalangeal syndrome I.

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Year:  1989        PMID: 2722199     DOI: 10.1007/BF00284059

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


  15 in total

1.  Tricho-rhino-phalangeal syndrome: report on three unrelated families.

Authors:  Y Sugiura; M Shionoya; T Inoue; T Tsuruta
Journal:  Jinrui Idengaku Zasshi       Date:  1976-06

2.  8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I.

Authors:  J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

3.  The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.

Authors:  P Bowen; B Biederman; J J Hoo
Journal:  Ann Genet       Date:  1985

Review 4.  Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.

Authors:  A P Walker; M Bocian
Journal:  Am J Med Genet       Date:  1987-05

5.  Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23----q21.1).

Authors:  F Shabtai; U Sandowski; R Nissimov; D Klar; I Halbrecht
Journal:  Clin Genet       Date:  1985-06       Impact factor: 4.438

6.  Familial tricho-rhino-phalangeal syndrome Type II.

Authors:  S Murachi; H Nogami; T Oki; T Ogino
Journal:  Clin Genet       Date:  1981-03       Impact factor: 4.438

7.  Tricho-rhino-phalangeal syndrome without exostoses, wih an interstitial deletion of 8q23.

Authors:  J Goldblatt; R D Smart
Journal:  Clin Genet       Date:  1986-05       Impact factor: 4.438

8.  A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.

Authors:  S Schwartz; J H Beisel; S R Panny; M M Cohen
Journal:  Clin Genet       Date:  1985-02       Impact factor: 4.438

9.  Chromosome deletion and multiple cartilaginous exostoses.

Authors:  E M Bühler; U K Bühler; G R Stalder; L Jani; L P Jurik
Journal:  Eur J Pediatr       Date:  1980-03       Impact factor: 3.183

10.  The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?

Authors:  E M Bühler; N J Malik
Journal:  Am J Med Genet       Date:  1984-09
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  4 in total

1.  SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variant.

Authors:  Andrew Dauber; Christelle Golzio; Cécile Guenot; Francine M Jodelka; Maria Kibaek; Susanne Kjaergaard; Bruno Leheup; Danielle Martinet; Malgorzata J M Nowaczyk; Jill A Rosenfeld; Susan Zeesman; Janice Zunich; Jacques S Beckmann; Joel N Hirschhorn; Michelle L Hastings; Sebastien Jacquemont; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2013-10-17       Impact factor: 11.025

Review 2.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

3.  Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression.

Authors:  Dezső David; Bárbara Marques; Cristina Ferreira; Carlos Araújo; Luís Vieira; Gabriela Soares; Cristina Dias; Maximina Pinto
Journal:  Hum Genet       Date:  2013-07-09       Impact factor: 4.132

Review 4.  Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements.

Authors:  Natalia V Kovaleva; Philip D Cotter
Journal:  Mol Cytogenet       Date:  2016-01-28       Impact factor: 2.009

  4 in total

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