Literature DB >> 4058983

Familial vocal cord dysfunction.

M J Cunningham, R D Eavey, D C Shannon.   

Abstract

Vocal cord paralysis is a common cause of neonatal stridor. Familial vocal cord dysfunction, however, is unusual. All three siblings in one family had neonatal stridor. Vocal cord dysfunction was confirmed after endoscopic examination in two of the children; a temporary tracheotomy was required by one child. Results of evaluation, including pulmonary function tests, suggest discrete dysfunction localized to the neuromuscular pathway responsible for vocal cord abduction. Endoscopy is of prime importance in the diagnosis of vocal cord dysfunction. In considering therapy, the physician must weigh both the potentially life-threatening nature of vocal cord paralysis, as well as the likelihood of eventual spontaneous resolution of many familial and idiopathic cases.

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Year:  1985        PMID: 4058983

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  3 in total

1.  FAMILIAL LARYNGEAL WEB IN THREE GENERATIONS WITH PROBABLE AUTOSOMAL DOMINANT TRANSMISSION.

Authors:  Stephen M Strakowski; Merlin G Butler; James W Cheek; William T Moore; James L Netterville; John A Phillips
Journal:  Dysmorphol Clin Genet       Date:  1988

2.  Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?

Authors:  E Boltshauser; W Lang; T Spillmann; E Hof
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

3.  Paradoxical vocal cord movement in newborn and congenital idiopathic vocal cord paralysis: two of a kind?

Authors:  Turid Omland; Kjell Brøndbo
Journal:  Eur Arch Otorhinolaryngol       Date:  2008-04-18       Impact factor: 2.503

  3 in total

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