Literature DB >> 6463801

Dysphagia in hypohidrotic ectodermal dysplasia. A case report.

P C Potter, M D Bowie.   

Abstract

The congenital ectodermal dysplasias are a rare group of hereditary disorders manifesting with variable defects in structures of ectodermal origin. This report describes a patient with the hypohidrotic form of ectodermal dysplasia who presented with dysphagia and pneumonia. He was shown to have laryngeal incompetence and it is postulated that this may be a mechanism for the recurrent chest infections reported in patients with this condition.

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Year:  1984        PMID: 6463801

Source DB:  PubMed          Journal:  S Afr Med J


  2 in total

1.  Oral surgery with nasotracheal intubation in a patient with ectodermal dysplasia.

Authors:  D Nanegrungsunk; B G Jericho
Journal:  Anaesth Rep       Date:  2020-07-23

2.  Multicore myopathy in a patient with anhidrotic ectodermal dysplasia.

Authors:  C P Gordon; S Litz
Journal:  Can J Anaesth       Date:  1992-11       Impact factor: 5.063

  2 in total

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