Literature DB >> 3776519

Mondini cochlea in Pendred's syndrome. A histological study.

T Johnsen, M B Jørgensen, S Johnsen.   

Abstract

In the past the Mondini malformation of the cochlea has been described histologically on the basis of findings in one temporal bone from a patient with confirmed Pendred's syndrome. The present study presents the histological examination of six temporal bones from 5 patients with confirmed Pendred syndrome. The characteristic Mondini cochlea was found in all preparations. It is concluded that the inner ear malformation in Pendred's syndrome is more in accordance with Mondini's original description than in other syndromes in which a Mondini-like cochlea has been described.

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Year:  1986        PMID: 3776519     DOI: 10.3109/00016488609108673

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  11 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.  Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential.

Authors:  Philine Wangemann
Journal:  J Physiol       Date:  2006-07-20       Impact factor: 5.182

Review 3.  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

4.  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

Review 5.  Cochlear histopathology in human genetic hearing loss: State of the science and future prospects.

Authors:  Krishna Bommakanti; Janani S Iyer; Konstantina M Stankovic
Journal:  Hear Res       Date:  2019-08-19       Impact factor: 3.208

6.  Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene.

Authors:  Guy Massa; Nele Jaenen; Sebastien Janssens de Varebeke; Nils Peeters; Wim Wuyts
Journal:  Eur J Pediatr       Date:  2003-08-15       Impact factor: 3.183

Review 7.  Congenital hearing impairment.

Authors:  Caroline D Robson
Journal:  Pediatr Radiol       Date:  2006-02-08

8.  Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.

Authors:  Ines E Royaux; Inna A Belyantseva; Tao Wu; Bechara Kachar; Lorraine A Everett; Daniel C Marcus; Eric D Green
Journal:  J Assoc Res Otolaryngol       Date:  2003-09

9.  Congenital goitrous hypothyroidism, deafness and iodide organification defect in four siblings: Pendred or pseudo-Pendred syndrome?

Authors:  Cengiz Kara; Mehtap Kılıç; Ahmet Uçaktürk; Murat Aydın
Journal:  J Clin Res Pediatr Endocrinol       Date:  2010-05-06

10.  Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.

Authors:  Akira Ganaha; Tadashi Kaname; Kumiko Yanagi; Kenji Naritomi; Tetsuya Tono; Shin-ichi Usami; Mikio Suzuki
Journal:  BMC Med Genet       Date:  2013-05-24       Impact factor: 2.103

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