Literature DB >> 25333908

Trichorhinophalangeal syndrome type I: a novel mutation and Perthes-like changes of the hip in a family with 4 cases over 3 generations.

Martin Hufeland1, Nils Rahner, Rüdiger Krauspe.   

Abstract

The trichorhinophalangeal syndrome is a rare genetic syndrome with characteristic craniofacial and skeletal abnormalities including hip pathology in variable manifestation. We describe hip involvement with Perthes-like changes and a novel mutation of the TRPSI gene in a family with 4 affected individuals. This case series underlines the clinical significance of rare genetic disorders such as TRPS that among other differential diagnoses should be kept in mind when children present with Perthes-like changes of the hip joint.

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Year:  2015        PMID: 25333908     DOI: 10.1097/BPO.0000000000000330

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  2 in total

Review 1.  Legg-Calvé-Perthes disease overview.

Authors:  Armando O Rodríguez-Olivas; Edgar Hernández-Zamora; Elba Reyes-Maldonado
Journal:  Orphanet J Rare Dis       Date:  2022-03-15       Impact factor: 4.123

2.  Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion.

Authors:  Qi Li; Zhen Zhang; Yuchun Yan; Ping Xiao; Zhijie Gao; Wei Cheng; Lin Su; Kaihui Yu; Hua Xie; Xiaoli Chen; Qian Jiang; Long Li
Journal:  Mol Cytogenet       Date:  2015-12-15       Impact factor: 2.009

  2 in total

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