Literature DB >> 2208762

Right-sided microtia and conductive hearing loss with variable expressivity in three generations.

K H Orstavik1, S Medbø, I W Mair.   

Abstract

Familial cases of microtia and meatal atresia are rare, and both dominant and recessive inheritance have been suggested. We here report a family with right-sided external ear malformations and conductive hearing loss in a grandfather, his daughter and granddaughter. The grandfather and the granddaughter both had microtia and meatal atresia, whereas the daughter had a normal outer ear except for a narrow meatus and auricular appendages. The pedigree suggests autosomal dominant inheritance with variable expressivity.

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Year:  1990        PMID: 2208762     DOI: 10.1111/j.1399-0004.1990.tb03558.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

Review 1.  Genetic Advances in the Understanding of Microtia.

Authors:  Craig Gendron; Ann Schwentker; John A van Aalst
Journal:  J Pediatr Genet       Date:  2016-09-23

Review 2.  Microtia: epidemiology and genetics.

Authors:  Daniela V Luquetti; Carrie L Heike; Anne V Hing; Michael L Cunningham; Timothy C Cox
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

3.  Optimising the decellularization of human elastic cartilage with trypsin for future use in ear reconstruction.

Authors:  Shafiq Rahman; Michelle Griffin; Anish Naik; Matthew Szarko; Peter E M Butler
Journal:  Sci Rep       Date:  2018-02-15       Impact factor: 4.379

  3 in total

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