Literature DB >> 3694034

Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.

T Johnsen1, C Larsen, J Friis, F Hougaard-Jensen.   

Abstract

Seventeen unrelated Danish patients with Pendred's syndrome, whose case stories have not been published previously, are presented. Acoustic and vestibular functions were examined and endocrinological screening was performed. There was a great variation in hearing ability as well as in thyroid function. Furthermore, in contrast to previous investigations, normal caloric function was demonstrated in the majority. In all patients a Mondini malformation was demonstrated. On the basis of this investigation it is concluded that: (1) the Mondini defect is part of Pendred's syndrome; (2) the inherited Mondini malformation is the underlying cause of the sensorineural hearing impairment; and (3) the hearing sensitivity varies greatly in these patients.

Entities:  

Mesh:

Year:  1987        PMID: 3694034     DOI: 10.1017/s0022215100103470

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  9 in total

1.  Thyroid function in patients with Pendred's syndrome.

Authors:  J Friis; T Johnsen; U Feldt-Rasmussen; K Bech; T Friis
Journal:  J Endocrinol Invest       Date:  1988-02       Impact factor: 4.256

Review 2.  Pendred syndrome.

Authors:  W Reardon; R C Trembath
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

Review 3.  Transcriptional regulation of the pendrin gene.

Authors:  Julia Rozenfeld; Edna Efrati; Lior Adler; Osnat Tal; Stephen L Carrithers; Seth L Alper; Israel Zelikovic
Journal:  Cell Physiol Biochem       Date:  2011-11-16

Review 4.  SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct.

Authors:  Taku Ito; Byung Yoon Choi; Kelly A King; Christopher K Zalewski; Julie Muskett; Parna Chattaraj; Thomas Shawker; James C Reynolds; John A Butman; Carmen C Brewer; Philine Wangemann; Seth L Alper; Andrew J Griffith
Journal:  Cell Physiol Biochem       Date:  2011-11-18

5.  Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear.

Authors:  L A Everett; H Morsli; D K Wu; E D Green
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

6.  Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.

Authors:  W Reardon; R Coffey; T Chowdhury; A Grossman; H Jan; K Britton; P Kendall-Taylor; R Trembath
Journal:  J Med Genet       Date:  1999-08       Impact factor: 6.318

7.  Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.

Authors:  Ruchira Singh; Philine Wangemann
Journal:  Am J Physiol Renal Physiol       Date:  2007-10-24

8.  Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family.

Authors:  Yock-Ping Chow; Nor Azian Abdul Murad; Zamzureena Mohd Rani; Jia-Shiun Khoo; Pei-Sin Chong; Loo-Ling Wu; Rahman Jamal
Journal:  Orphanet J Rare Dis       Date:  2017-02-21       Impact factor: 4.123

Review 9.  The unique electrical properties in an extracellular fluid of the mammalian cochlea; their functional roles, homeostatic processes, and pathological significance.

Authors:  Fumiaki Nin; Takamasa Yoshida; Seishiro Sawamura; Genki Ogata; Takeru Ota; Taiga Higuchi; Shingo Murakami; Katsumi Doi; Yoshihisa Kurachi; Hiroshi Hibino
Journal:  Pflugers Arch       Date:  2016-08-27       Impact factor: 3.657

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.