Literature DB >> 3997376

Meatal atresia and hearing loss. Autosomal dominant and autosomal recessive inheritance.

C W Cremers.   

Abstract

Thirty-six ears of 33 patients with a type II unilateral or bilateral meatal atresia were accepted for reconstructive surgery. Five families of these patients had a history of congenital aural atresia. In one the father and his son had unilateral microtia. Four families counted 2 affected sibs each. The autosomal dominant and autosomal recessive patterns of inheritance are discussed.

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Year:  1985        PMID: 3997376     DOI: 10.1016/s0165-5876(85)80081-1

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  3 in total

1.  Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans.

Authors:  Ilse Feenstra; Lisenka E L M Vissers; Ronald J E Pennings; Willy Nillessen; Rolph Pfundt; Henricus P Kunst; Ronald J Admiraal; Joris A Veltman; Conny M A van Ravenswaaij-Arts; Han G Brunner; Cor W R J Cremers
Journal:  Am J Hum Genet       Date:  2011-12-09       Impact factor: 11.025

2.  Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia.

Authors:  J Mortier; J van den Ende; F Declau; H Vercruysse; W Wuyts; G Van Camp; O Vanderveken; An Boudewyns
Journal:  Eur Arch Otorhinolaryngol       Date:  2022-06-27       Impact factor: 2.503

3.  Microtia: A Data Linkage Study of Epidemiology and Implications for Service Delivery.

Authors:  Thomas H Jovic; John A G Gibson; Rowena Griffiths; Thomas D Dobbs; Ashley Akbari; Nicholas Wilson-Jones; Rhodri Costello; Peter Evans; Mark Cooper; Steve Key; Ronan Lyons; Iain S Whitaker
Journal:  Front Pediatr       Date:  2021-03-26       Impact factor: 3.418

  3 in total

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