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Autosomal Recessive Sensorineural Hearing Impairment, Dizziness, and Hypodontia

Autosomal Recessive Sensorineural Hearing Impairment, Dizziness, and Hypodontia Abstract • A previously undescribed syndrome with profound sensorineural hearing loss since early infancy, episodes of dizziness, and hypodontia developed in a brother and sister. The presence of two unaffected children and unaffected parents suggests autosomal recessive inheritance. (Arch Otolaryngol 104:292-293, 1978) References 1. Levin LS, Jorgenson RJ, Cook RA: Otodental dysplasia: A "new" ectodermal dysplasia . Clin Genet 8:136-144, 1975.Crossref 2. Hollister DW, Klein SH, DeJager NJ, et al: The lacrimo-auriculo-dento-digital syndrome . J Pediatr 83:438-444, 1973.Crossref 3. Robinson GC, Miller JR, Bensimon JR: Familial ectodermal dysplasia with sensorineural deafness and other anomalies . Pediatrics 30:797-802, 1962. 4. Fraser GR: The Causes of Profound Deafness in Childhood . Baltimore, The Johns Hopkins Press, 1976, pp 11-35. 5. Fraser GR: Association of congenital deafness with goitre (Pendred's syndrome): A study of 207 families . Ann Hum Genet 28:201-249, 1965.Crossref 6. Kongismark BW, Gorlin RJ: Genetic and Metabolic Deafness . Philadelphia, WB Saunders Co, 1976. 7. Nuutila A: Dystrophia retinae pigmentosadysacusis syndrome (DRD): A study of the Usher or Hallgren syndrome . J Genet Hum 18:57-88, 1970. 8. McLeod AC, McConnell FE, Sweeney A, et al: Clinical variation in Usher's syndrome . Arch Otolaryngol 94:321-334, 1971.Crossref 9. Jervell A, Lange-Nielson F: Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death . Am Heart J 54:59-68, 1957.Crossref 10. Witkop CJ, Brearley LJ, Gentry WC Jr: Hypoplastic enamel, onycholysis, and hypohydroses inherited as an autosomal dominant trait: A review of ectodermal dysplasia syndromes . Oral Surg 39:71-86, 1975.Crossref 11. Basser LS: Benign paroxysmal vertigo of childhood . Brain 87:141-152, 1964.Crossref http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Otolaryngology American Medical Association

Autosomal Recessive Sensorineural Hearing Impairment, Dizziness, and Hypodontia

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Publisher
American Medical Association
Copyright
Copyright © 1978 American Medical Association. All Rights Reserved.
ISSN
0003-9977
DOI
10.1001/archotol.1978.00790050058013
Publisher site
See Article on Publisher Site

Abstract

Abstract • A previously undescribed syndrome with profound sensorineural hearing loss since early infancy, episodes of dizziness, and hypodontia developed in a brother and sister. The presence of two unaffected children and unaffected parents suggests autosomal recessive inheritance. (Arch Otolaryngol 104:292-293, 1978) References 1. Levin LS, Jorgenson RJ, Cook RA: Otodental dysplasia: A "new" ectodermal dysplasia . Clin Genet 8:136-144, 1975.Crossref 2. Hollister DW, Klein SH, DeJager NJ, et al: The lacrimo-auriculo-dento-digital syndrome . J Pediatr 83:438-444, 1973.Crossref 3. Robinson GC, Miller JR, Bensimon JR: Familial ectodermal dysplasia with sensorineural deafness and other anomalies . Pediatrics 30:797-802, 1962. 4. Fraser GR: The Causes of Profound Deafness in Childhood . Baltimore, The Johns Hopkins Press, 1976, pp 11-35. 5. Fraser GR: Association of congenital deafness with goitre (Pendred's syndrome): A study of 207 families . Ann Hum Genet 28:201-249, 1965.Crossref 6. Kongismark BW, Gorlin RJ: Genetic and Metabolic Deafness . Philadelphia, WB Saunders Co, 1976. 7. Nuutila A: Dystrophia retinae pigmentosadysacusis syndrome (DRD): A study of the Usher or Hallgren syndrome . J Genet Hum 18:57-88, 1970. 8. McLeod AC, McConnell FE, Sweeney A, et al: Clinical variation in Usher's syndrome . Arch Otolaryngol 94:321-334, 1971.Crossref 9. Jervell A, Lange-Nielson F: Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death . Am Heart J 54:59-68, 1957.Crossref 10. Witkop CJ, Brearley LJ, Gentry WC Jr: Hypoplastic enamel, onycholysis, and hypohydroses inherited as an autosomal dominant trait: A review of ectodermal dysplasia syndromes . Oral Surg 39:71-86, 1975.Crossref 11. Basser LS: Benign paroxysmal vertigo of childhood . Brain 87:141-152, 1964.Crossref

Journal

Archives of OtolaryngologyAmerican Medical Association

Published: May 1, 1978

References