Literature DB >> 6496574

The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature.

L O Langer, N Krassikoff, R Laxova, M Scheer-Williams, L D Lutter, R J Gorlin, C G Jennings, D W Day.   

Abstract

We report on four patients with tricho-rhino-phalangeal syndrome with exostoses (TRPSE) who were not mentally retarded and review 32 previously published cases. These data enable more complete delineation of the phenotype and document the variability of the clinical and radiographic manifestations. Information on the genetics and the association with del(8q) is discussed, as are management and avenues for further investigation. The apparent variability of intelligence in TRPSE patients together with the high incidence of other problems, including significant delay in speech development and hearing loss, make systematic multidisciplinary evaluation and long-term treatment necessary to achieve the best outcome.

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Year:  1984        PMID: 6496574     DOI: 10.1002/ajmg.1320190110

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  24 in total

1.  The tricho-rhino-phalangeal syndromes I and II.

Authors:  L Mehta; P K Jain; R Saxena; I C Verma
Journal:  Indian J Pediatr       Date:  1992 May-Jun       Impact factor: 1.967

Review 2.  International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone.

Authors:  J Spranger
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

3.  Multiple exostoses in a patient with t(8;11)(q24.11;p15.5).

Authors:  R F Ogle; P Dalzell; G Turner; D Wass; M Y Yip
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

4.  Hereditary multiple exostoses.

Authors:  R C Hennekam
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

5.  Haematometra in the Langer-Giedion syndrome.

Authors:  M W Partington; J Rae; M J Payne
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

6.  Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome.

Authors:  H J Lüdecke; R Burdiek; G Senger; U Claussen; E Passarge; B Horsthemke
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

Review 7.  Human chromosome 8.

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

8.  Tricho-rhino-phalangeal syndrome type I in a Belgian family.

Authors:  L A Verbruggen; C Van Laere; J Lamoureux; R Van Tiggelen
Journal:  Clin Rheumatol       Date:  1987-06       Impact factor: 2.980

Review 9.  Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.

Authors:  A H Lipson; D Yuille; M Angel; P G Thompson; J G Vandervoord; E J Beckenham
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

10.  Molecular studies of DiGeorge syndrome.

Authors:  W J Fibison; M Budarf; H McDermid; F Greenberg; B S Emanuel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

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