Literature DB >> 25821091

The neuromuscular differential diagnosis of joint hypermobility.

S Donkervoort, C G Bonnemann, B Loeys, H Jungbluth, N C Voermans.   

Abstract

Joint hypermobility is the defining feature of various inherited connective tissue disorders such as Marfan syndrome and various types of Ehlers-Danlos syndrome and these will generally be the first conditions to be considered by geneticists and pediatricians in the differential diagnosis of a patient presenting with such findings. However, several congenital and adult-onset inherited myopathies also present with joint hypermobility in the context of often only mild-to-moderate muscle weakness and should, therefore, be included in the differential diagnosis of joint hypermobility. In fact, on the molecular level disorders within both groups represent different ends of the same spectrum of inherited extracellular matrix (ECM) disorders. In this review we will summarize the measures of joint hypermobility, illustrate molecular mechanisms these groups of disorders have in common, and subsequently discuss the clinical features of: 1) the most common connective tissue disorders with myopathic or other neuromuscular features: Ehlers-Danlos syndrome, Marfan syndrome and Loeys-Dietz syndrome; 2) myopathy and connective tissue overlap disorders (muscle extracellular matrix (ECM) disorders), including collagen VI related dystrophies and FKBP14 related kyphoscoliotic type of Ehlers-Danlos syndrome; and 3) various (congenital) myopathies with prominent joint hypermobility including RYR1- and SEPN1-related myopathy. The aim of this review is to assist clinical geneticists and other clinicians with recognition of these disorders.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  extracellular matrix; hypermobility; inherited connective tissue disorders; myopathies

Mesh:

Year:  2015        PMID: 25821091     DOI: 10.1002/ajmg.c.31433

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  5 in total

1.  Proximal Limb Girdle Weakness, Joint Hyperlaxity, and preserved Deep Tendon Reflexes: A Distinctive Phenotype.

Authors:  Priyanka Madaan; Lokesh Saini
Journal:  Indian Pediatr       Date:  2020-10-15       Impact factor: 1.411

2.  P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.

Authors:  Yaqun Zou; Sandra Donkervoort; Antti M Salo; A Reghan Foley; Aileen M Barnes; Ying Hu; Elena Makareeva; Meganne E Leach; Payam Mohassel; Jahannaz Dastgir; Matthew A Deardorff; Ronald D Cohn; Wendy O DiNonno; Fransiska Malfait; Monkol Lek; Sergey Leikin; Joan C Marini; Johanna Myllyharju; Carsten G Bönnemann
Journal:  Hum Mol Genet       Date:  2017-06-15       Impact factor: 6.150

Review 3.  Review of RyR1 pathway and associated pathomechanisms.

Authors:  Jessica W Witherspoon; Katherine G Meilleur
Journal:  Acta Neuropathol Commun       Date:  2016-11-17       Impact factor: 7.801

4.  Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands.

Authors:  Stacha F I Reumers; Corrie E Erasmus; Karlijn Bouman; Maartje Pennings; Meyke Schouten; Benno Kusters; Floor A M Duijkers; Anneke van der Kooi; Bregje Jaeger; Corien C Verschuuren-Bemelmans; Catharina G Faber; Baziel G van Engelen; Erik-Jan Kamsteeg; Heinz Jungbluth; Nicol C Voermans
Journal:  Clin Genet       Date:  2021-09-25       Impact factor: 4.296

5.  Transcriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type.

Authors:  Nicola Chiarelli; Giulia Carini; Nicoletta Zoppi; Chiara Dordoni; Marco Ritelli; Marina Venturini; Marco Castori; Marina Colombi
Journal:  PLoS One       Date:  2016-08-12       Impact factor: 3.240

  5 in total

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