Literature DB >> 15843272

A new syndrome of myopathy with muscle spindle excess.

Stephani Stassou1, Ali Nadroo, Romaine Schubert, Steven Chin, Madhu Gudavalli.   

Abstract

Arthrogryposis may result from various neuromuscular or connective tissue disorders leading to in utero hypokinesia or akinesia and the prenatal development of joint contractures. We report the case of a preterm neonate born with arthrogryposis and flaccid quadriplegia that led to the diagnosis of myopathy with muscle spindle excess. The rare and unusual histopathologic abnormality associated with the myopathy illustrated in this case has been described in only three other cases in the medical literature. The concurrence of hypertrophic cardiomyopathy, arthrogryposis, and myopathy with muscle spindle excess suggests the presence of a newly described syndrome. This case clearly demonstrates that specific prenatal ultrasonographic findings combined with the presenting clinical manifestations should promptly raise the suspicion of a neuromuscular disorder.

Entities:  

Mesh:

Year:  2005        PMID: 15843272     DOI: 10.1515/JPM.2005.034

Source DB:  PubMed          Journal:  J Perinat Med        ISSN: 0300-5577            Impact factor:   1.901


  4 in total

1.  A rare case of congenital myopathy with excess muscle spindles: expanding the clinical spectrum of HRAS-associated neuromuscular disease.

Authors:  Julia M Henry; Nizar Chahin; Yael Shiloh-Malawsky; Zheng Fan; Duygu Selcen
Journal:  J Neurol       Date:  2015-05-23       Impact factor: 4.849

Review 2.  A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Authors:  Anne H Mardy; Shilpa P Chetty; Mary E Norton; Teresa N Sparks
Journal:  Prenat Diagn       Date:  2019-06-26       Impact factor: 3.050

3.  Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation.

Authors:  Ineke van der Burgt; William Kupsky; Stephani Stassou; Ali Nadroo; Cândida Barroso; Angelika Diem; Christian P Kratz; Radovan Dvorsky; Mohammad Reza Ahmadian; Martin Zenker
Journal:  J Med Genet       Date:  2007-04-05       Impact factor: 6.318

4.  Genetic diagnosis and clinical evaluation of severe fetal akinesia syndrome.

Authors:  Theresa Reischer; Sandra Liebmann-Reindl; Dieter Bettelheim; Sukirthini Balendran-Braun; Berthold Streubel
Journal:  Prenat Diagn       Date:  2020-09-10       Impact factor: 3.050

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.