International Journal of Pediatric Otorhinolaryngology
Volume 67, Issue 4 , Pages 427-428 , April 2003

Hereditary vocal cord palsy

Received 11 July 2002 ,Revised 14 November 2002 ,Accepted 16 November 2002.

References 

  1. Manligod JM, Smith RJ. Familial laryngeal paralysis. Am. J. Med. Genet. 1988;77(4):277–280
  2. Morelli G, Mesolella C, Costa F, Testa B, Ventruto B, Santulli S. Familial laryngeal abductor paralysis with presumed autosomal dominant inheritance. Ann. Otol. Rhinol. Laryngol. 1982;91(3 Pt 1):323–324
  3. Donaghy M, Kennet R. Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy. J. Neurol. 1999;246(7):552–555
  4. Boltshauser E, Lang W, Spillman T, Hof E. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?. J. Med. Genet. 1989;26:105–108
  5. Manaligod JM, Skaggs , Smith RJ. Localisation of the gene for familial laryngeal abductor paralysis to chromosome 6q16. Arch. Otolaryngol. Head Neck Surg. 2001;127(8):913–917
  6. Skre H. Genetic and clinical aspects of Charcot–Marie–tooth disease. Clin. Genet. 1974;6:98–118
  7. Schinzel A, Hof E, Dangel P, Robinson W. Familial congenital laryngeal abductor paralysis: different expressions in a family with one male and three females affected. J. Med. Genet. 1990;27(11):715–716
  8. Mace M, Williamson E, Morgan D. Autosomal dominantly inherited adductor laryngeal paralysis—a new syndrome with suggestion of linkage to HLA. Clin. Genet. 1978;14:265–270

PII: S0165-5876(02)00398-1

doi: 10.1016/S0165-5876(02)00398-1

International Journal of Pediatric Otorhinolaryngology
Volume 67, Issue 4 , Pages 427-428 , April 2003

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