Literature DB >> 32024714

Ehlers-Danlos syndrome presenting with primary nocturnal enuresis.

Margarida Cunha1, Mafalda Matias2, Inês Marques2.   

Abstract

Ehlers-Danlos syndrome (EDS), hypermobility type, is probably the most common EDS type, as well as the most common heritable connective tissue disorder. Bladder dysfunction is a rare clinical manifestation of EDS and manifests itself as primary nocturnal enuresis. We present a 10-year-old boy referred to the paediatrics nephrology consultation due to primary nocturnal enuresis and day time symptoms of urinary urgency. During the appointment, a tendency to joint hypermobility was noted. On evaluation the skin was hyperextensible and the Beighton score was positive. The genetic testing revealed a variant of the COL5A1 gene not yet described in the literature. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  congenital disorders; connective tissue disease; genetic screening/counselling; musculoskeletal and joint disorders; urinary and genital tract disorders

Mesh:

Substances:

Year:  2020        PMID: 32024714      PMCID: PMC7021119          DOI: 10.1136/bcr-2019-231977

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


  4 in total

1.  Generalized joint hypermobility and voiding dysfunction in children: is there any relationship?

Authors:  Abdol-Mohammad Kajbafzadeh; Lida Sharifi-Rad; Seyedeh Sanam Ladi Seyedian; Sarah Mozafarpour; Koosha Paydary
Journal:  Eur J Pediatr       Date:  2014-02       Impact factor: 3.183

Review 2.  Contemporary approach to joint hypermobility and related disorders.

Authors:  Marco Castori; Alan Hakim
Journal:  Curr Opin Pediatr       Date:  2017-12       Impact factor: 2.856

3.  Lower urinary tract dysfunction in children with generalized hypermobility of joints.

Authors:  Laetitia M O de Kort; John A P M Verhulst; Raoul H H Engelbert; Cuno S P M Uiterwaal; Tom P V M de Jong
Journal:  J Urol       Date:  2003-11       Impact factor: 7.450

4.  Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations.

Authors:  Marco Castori
Journal:  ISRN Dermatol       Date:  2012-11-22
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.