2010, Number 3
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Otorrinolaringología 2010; 55 (3)
Otological diseases in patients with genetic syndromes and congenital malformations: experience at Hospital Juarez of Mexico
Beltrán ZE, Juárez NOJ
Language: Spanish
References: 12
Page: 97-100
PDF size: 667.84 Kb.
ABSTRACT
The distinct genetic syndromes and congenital malformations present a wide variety of alterations, most frequently of the craniofacial type, and among these, the ear is no exempt to the latter. In Hospital Juárez, as a reference hospital and a center with a predominance of otologic pathology, we have a great number of cases, and a lot of these are treated at the Otolaryngology an Head and Neck Surgery and audiology department. We decided to do a thorough analysis of the most frequent pathologies at our center, their treatment and evolution. We did an analytic, non-invasive, case review study.
REFERENCES
Gorlin A, Toriello H, Cohen M. Hereditary hearing loss and its syndromes. New York: Oxford University Press, 1995.
Sacks B, Wood A. Hearing disorders in children with Down syndrome. Down Syndrome News and Update 2003;3(2):38 41.
Bacciu A, Pasanisi E, Vincenti V. Surgical treatment of middle ear cholesteatoma in children with Down syndrome. Otol Neurotol 2005;26:1007-10.
Jahrsdoerfer RA, Yeakley JW, Aguilar EA. Grading system for the selection of patients with congenital aural atresia. Am J Otol 1992;13:6-12.
Nishizaki K, Masuda Y, Karita K. Management and its post-operative complications in congenital aural atresia. Acta Oto-laryngologica 1999;119(540):42-44.
Chandrasekhar SS, De la Cruz A, Garrido E. Surgery of congenital aural atresia. Am J Otol 1995;16:713-717.
Jahrsdoerfer RA, Lambert PR. Facial nerve injury in congenital aural atresia surgery. Am J Otol 1998;19:283-287.
American Cleft Palate Association. Parameters for evaluation and treatment of patients with cleft lip/palate or other craniofacial anomalies. Cleft Palate Craniofac J 1993;30:S1.
Jacobsson C, Granstrom G. Clinical appearance of spontaneous and induced first and second branchial arch syndromes. Scand J Plast Reconstr Surg Hand Surg 1997;31:125-136.
Ari-Even Roth D, Hildesheimer M. Preauricular skin tags and ear pits are associated with permanent hearing impairment in newborns. Pediatrics 2008;122(4):884-890.
Cremers CWRJ, Fikkers-van Noord M. The earpitsdeafness syndrome. Clinical and genetic aspects. Int J Pediatr Otorhinolaryngol 1980;2:309-322.
Fraser FC, Ling D, Clogg D, et al. Genetic aspects of the BOR syndrome-branchial fistulas, ear pits, hearing loss and renal anomalies. Am J Med Genet 1978;2:241-252.