Analysis of the thyroid phenotype in 42 patients with pendred syndrome and nonsyndromic enlargement of the vestibular aqueduct

Thyroid

Volumn 24, Issue 4, 2014, Pages 639-648

  Ladsous, Miriam ^a   Vlaeminck Guillem, Virginie ^a,b   Dumur, Viviane ^a   Vincent, Christophe ^a   Dubrulle, Frédérique ^a   Dhaenens, Claire Marie ^a,c   Wémeau, Jean Louis ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b UNIVERSITÉ LYON 1   (France)

^c UNIV LILLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PENDRIN; THYROGLOBULIN; CARRIER PROTEIN; SLC26A4 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUDITORY SYSTEM EXAMINATION; CHILD; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL HYPOTHYROIDISM; ECHOGRAPHY; FAMILY; FEMALE; GENE; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; GOITER; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUMAN TISSUE; HYPOTHYROIDISM; INNER EAR; MALE; MUTATIONAL ANALYSIS; NODULAR GOITER; NUCLEAR MAGNETIC RESONANCE IMAGING; PENDRED SYNDROME; PERCEPTION DEAFNESS; PERCHLORATE DISCHARGE TEST; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SCHOOL CHILD; SLC26A4 GENE; SUBCLINICAL HYPOTHYROIDISM; THYROID FUNCTION TEST; THYROID SCINTISCANNING; VESTIBULAR DISORDER; VESTIBULE AQUEDUCT; VESTIBULE AQUEDUCT ENLARGEMENT; YOUNG ADULT; GENETIC ASSOCIATION; GENETICS; GOITER, NODULAR; HEARING LOSS, SENSORINEURAL; MIDDLE AGED; MUTATION; PATHOLOGY; PHENOTYPE; PRESCHOOL CHILD; THYROID GLAND;

ADOLESCENT; ADULT; ALLELES; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC ASSOCIATION STUDIES; GOITER; GOITER, NODULAR; HEARING LOSS, SENSORINEURAL; HETEROZYGOTE; HOMOZYGOTE; HUMANS; HYPOTHYROIDISM; MALE; MEMBRANE TRANSPORT PROTEINS; MIDDLE AGED; MUTATION; PHENOTYPE; THYROID GLAND; VESTIBULAR AQUEDUCT; YOUNG ADULT;

EID: 84898466838     PISSN: 10507256     EISSN: 15579077     Source Type: Journal    
DOI: 10.1089/thy.2013.0164     Document Type: Article

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