Literature DB >> 24881034

Accessory limb with myelomeningocele: a rare case challenging previously held beliefs.

Christopher Parks1, John Mugamba.   

Abstract

INTRODUCTION: There have been previous reports of intra-scapular limbs associated with a closed spina bifida and this has led to a causative theory. It is thought that these dysraphic appendages could not occur with defects of primary neurulation. CASE: The authors present a rare case of this abnormality associated with a large open myelomeningocele in a 6-day-old infant presenting to a paediatric neurosurgical hospital in Uganda. The appendage was removed and the spina bifida closed. There was significant stigma associated with such abnormality in this region. DISCUSSION: The first reported co-existence of these two lesions challenges previously held beliefs regarding the embryological origin of intra-scapular dysraphic appendage.

Entities:  

Mesh:

Year:  2014        PMID: 24881034     DOI: 10.1007/s00381-014-2452-1

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  2 in total

Review 1.  Accessory limbs associated with spina bifida - a second look.

Authors:  A Krishna; P Lal
Journal:  Pediatr Surg Int       Date:  1999       Impact factor: 1.827

2.  Hypothesis; overdistention of the neural tube may cause anomalies of non-neural organs.

Authors:  W J Gardner
Journal:  Teratology       Date:  1980-10
  2 in total
  2 in total

Review 1.  Notomelia and related neural tube defects in a baby born in Niger: case report and literature review.

Authors:  A B Kelani; H Moumouni; A W Issa; H Younsaa; Hmu Fokou; R Sani; S Sanoussi; L J Denholm; J E Beever; M Catala
Journal:  Childs Nerv Syst       Date:  2017-01-12       Impact factor: 1.475

2.  Proposed caudal appendage classification system; spinal cord tethering associated with sacrococcygeal eversion.

Authors:  C Corbett Wilkinson; Arianne J Boylan
Journal:  Childs Nerv Syst       Date:  2016-08-06       Impact factor: 1.475

  2 in total

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