Literature DB >> 3742850

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

J Goldblatt, R D Smart.   

Abstract

We report on a patient with the Tricho-Rhino-Phalangeal syndrome (TRPS) with normal mentation, without exostoses and with a partial microdeletion of 8q23. Although she had the phenotypic characteristics of TRPS Type I, karyotypic analysis demonstrated the 8q-microdeletion usually associated with TRPS Type II, in which exostoses are present. Our patient represents the second reported instance of this phenotypic chromosomal association and provides further evidence for homogeneity of the TRPS.

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Year:  1986        PMID: 3742850     DOI: 10.1111/j.1399-0004.1986.tb00517.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

Review 1.  Human chromosome 8.

Authors:  S Wood
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

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

Authors:  K Naritomi; K Hirayama
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

Review 3.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

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

Review 4.  Microdeletion syndromes, balanced translocations, and gene mapping.

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

5.  The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).

Authors:  M Le Merrer; K Ben Othmane; V Stanescu; S Lyonnet; L Van Maldergem; G Royer; A Munnich; P Maroteaux
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

6.  Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.

Authors:  W Wuyts; S Ramlakhan; W Van Hul; J T Hecht; A M van den Ouweland; W H Raskind; F C Hofstede; E Reyniers; D E Wells; B de Vries
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

7.  Disorders caused by chromosome abnormalities.

Authors:  Aaron Theisen; Lisa G Shaffer
Journal:  Appl Clin Genet       Date:  2010-12-10
  7 in total

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