Literature DB >> 12210298

Diagnostic dilemmas in the short rib-polydactyly syndrome group.

Nursel H Elçioglu1, Christine M Hall.   

Abstract

The short rib-polydactyly syndromes are a group of lethal skeletal dysplasias with autosomal recessive inheritance characterized by markedly short ribs, short limbs, usually polydactyly, and multiple anomalies of major organs. At least four types have been recognized. The radiological findings of 10 cases are presented. Each fetus or stillbirth has some of the radiological features of the four established types of short rib-polydactyly syndrome and raises diagnostic dilemmas in differentiating these entities. The overlapping phenotypes of these fetuses supports the previously suggested hypothesis that the different subtypes of the short rib-polydactyly syndrome group are not single entities, but rather part of a continuous spectrum with variable expressivity. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2002        PMID: 12210298     DOI: 10.1002/ajmg.10562

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


  7 in total

1.  Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.

Authors:  Amy E Merrill; Barry Merriman; Claire Farrington-Rock; Natalia Camacho; Eiman T Sebald; Vincent A Funari; Matthew J Schibler; Marc H Firestein; Zachary A Cohn; Mary Ann Priore; Alicia K Thompson; David L Rimoin; Stanley F Nelson; Daniel H Cohn; Deborah Krakow
Journal:  Am J Hum Genet       Date:  2009-04       Impact factor: 11.025

2.  Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan type.

Authors:  N Badiner; S P Taylor; K Forlenza; R S Lachman; M Bamshad; D Nickerson; D H Cohn; D Krakow
Journal:  Clin Genet       Date:  2017-03-13       Impact factor: 4.438

3.  NEK1 mutations cause short-rib polydactyly syndrome type majewski.

Authors:  Christian Thiel; Kristin Kessler; Andreas Giessl; Arno Dimmler; Stavit A Shalev; Sigrun von der Haar; Martin Zenker; Diana Zahnleiter; Hartmut Stöss; Ernst Beinder; Rami Abou Jamra; Arif B Ekici; Nadja Schröder-Kress; Thomas Aigner; Thomas Kirchner; André Reis; Johann H Brandstätter; Anita Rauch
Journal:  Am J Hum Genet       Date:  2011-01-07       Impact factor: 11.025

4.  A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis.

Authors:  Xiaoqian Ye; Guangtai Song; Mingwen Fan; Lisong Shi; Ethylin Wang Jabs; Shangzhi Huang; Ruiqiang Guo; Zhuan Bian
Journal:  Hum Genet       Date:  2006-01-11       Impact factor: 4.132

5.  DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects.

Authors:  Kristin Kessler; Ina Wunderlich; Steffen Uebe; Nathalie S Falk; Andreas Gießl; Johann Helmut Brandstätter; Bernt Popp; Patricia Klinger; Arif B Ekici; Heinrich Sticht; Helmuth-Günther Dörr; André Reis; Ronald Roepman; Eva Seemanová; Christian T Thiel
Journal:  Sci Rep       Date:  2015-07-01       Impact factor: 4.379

6.  Whole-exome sequencing identified two novel mutations of DYNC2LI1 in fetal skeletal ciliopathy.

Authors:  Xinyue Zhang; Yanqin You; Xiaoxiao Xie; Hong Xu; Honghui Zhou; Yuanmei Lei; Pei Sun; Yuanguang Meng; Longxia Wang; Yanping Lu
Journal:  Mol Genet Genomic Med       Date:  2020-10-08       Impact factor: 2.183

Review 7.  Ellis-van Creveld syndrome.

Authors:  Geneviève Baujat; Martine Le Merrer
Journal:  Orphanet J Rare Dis       Date:  2007-06-04       Impact factor: 4.123

  7 in total

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