Literature DB >> 4017280

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

F Shabtai, U Sandowski, R Nissimov, D Klar, I Halbrecht.   

Abstract

A family is reported with an autosomal dominant inherited syndrome presenting some of the typical features of the tricho-rhino-phalangeal syndrome type II (TRP II) or Langer-Giedion syndrome. The critical region for the expression of the syndrome seems to be at band 8q24.1. In the affected members of the family reported here, anomaly of chromosome 8 was noted, involving however the proximal part of the 8 long arm, which was interpreted as a paracentric inversion. Whether the anomaly is causally or only casually related to the syndrome is a matter of discussion.

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Year:  1985        PMID: 4017280     DOI: 10.1111/j.1399-0004.1985.tb02045.x

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


  6 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

Review 5.  Paracentric inversions: a review.

Authors:  K Madan
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

6.  Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.

Authors:  H J Lüdecke; C Johnson; M J Wagner; D E Wells; C Turleau; N Tommerup; A Latos-Bielenska; K R Sandig; P Meinecke; B Zabel
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

  6 in total

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