Literature DB >> 31068350

Lethal multiple pterygium syndrome.

Farzeen Shuaib Mohtisham1,2, Adel Sallam1,2, Aiman Shawli2,3.   

Abstract

Multiple pterygium syndrome of lethal type is a very rare genetic condition affecting the skin, muscles and skeleton. It is characterised by minor facial abnormalities, prenatal growth deficiency, spine defects, joint contractures, and webbing (pterygia) of the neck, elbows, back of the knees, armpits and fingers. We present a case of lethal multiple pterygium syndrome born at our hospital proven by the genetic analysis showing a double homozygous mutation. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  congenital disorders; genetic screening / counselling; musculoskeletal syndromes; neonatal intensive care

Mesh:

Substances:

Year:  2019        PMID: 31068350      PMCID: PMC6506140          DOI: 10.1136/bcr-2018-229045

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  4 in total

1.  Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.

Authors:  Neil V Morgan; Louise A Brueton; Phillip Cox; Marie T Greally; John Tolmie; Shanaz Pasha; Irene A Aligianis; Hans van Bokhoven; Tamas Marton; Lihadh Al-Gazali; Jenny E V Morton; Christine Oley; Colin A Johnson; Richard C Trembath; Han G Brunner; Eamonn R Maher
Journal:  Am J Hum Genet       Date:  2006-06-20       Impact factor: 11.025

2.  The lethal multiple pterygium syndromes.

Authors:  J G Hall
Journal:  Am J Med Genet       Date:  1984-04

3.  Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.

Authors:  Julie Vogt; Benjamin J Harrison; Hayley Spearman; Judy Cossins; Sascha Vermeer; Lambert Naudin ten Cate; Neil V Morgan; David Beeson; Eamonn R Maher
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

4.  Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum.

Authors:  Ariana Kariminejad; Siavash Ghaderi-Sohi; Hamid Hossein-Nejad Nedai; Vahid Varasteh; Ali-Reza Moslemi; Homa Tajsharghi
Journal:  BMC Musculoskelet Disord       Date:  2016-03-01       Impact factor: 2.362

  4 in total
  1 in total

1.  Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report.

Authors:  Jianlong Zhuang; Junyu Wang; Qi Luo; Shuhong Zeng; Yu'e Chen; Yuying Jiang; Xinying Chen; Yuanbai Wang; Yingjun Xie; Gaoxiong Wang; Chunnuan Chen
Journal:  Front Genet       Date:  2022-08-26       Impact factor: 4.772

  1 in total

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