Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome

International Journal of Pediatric Otorhinolaryngology

Volumn 45, Issue 2, 1998, Pages 113-123

  Cremers, Cor W R J ^a   Admiraal, Ronald J C ^a   Huygen, Patrick L M ^a   Bolder, Cuny ^a   Everett, Lorraine A ^b   Joosten, Frank B M ^a   Green, Eric D ^b   Van Camp, Guy ^b   Otten, Barto J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b Univ Hosp PO Box 9101 6500 H ^*

Author keywords

Autosomal recessive; Childhood deafness; Enlarged vestibular aqueduct; Genetic deafness; Mondini's dysplasia; PDS gene; Pendred's syndrome; Sensorineural hearing loss; Widened vestibular aqueduct

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUDIOGRAPHY; CLINICAL ARTICLE; FAMILY HISTORY; FEMALE; GENE MUTATION; GOITER; HEARING LOSS; HUMAN; INNER EAR DISEASE; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PENDRED SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; TEMPORAL BONE; VESTIBULAR TEST; VESTIBULE AQUEDUCT;

CHILD; CHILD, PRESCHOOL; COCHLEA; DNA MUTATIONAL ANALYSIS; FEMALE; FOLLOW-UP STUDIES; GOITER; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MALE; PHENOTYPE; REGRESSION ANALYSIS; SYNDROME; TIME FACTORS; VESTIBULAR AQUEDUCT;

EID: 0032476116     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(98)00123-2     Document Type: Article

References (15)

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