Literature DB >> 11807445

Three members of a family with pili torti and sensorineural hearing loss: the Bjornstad syndrome.

Kristen A Richards1, Anthony J Mancini.   

Abstract

Thirty cases of the Bjornstad syndrome (sensorineural deafness and pili torti) have been reported between 1965, when it was first described, and 1999. Both autosomal dominant and recessive inheritance patterns appear in the literature. We describe a family in which 3 members have the combination of pili torti and varying degrees of hearing loss inherited in an apparently autosomal dominant fashion. Hairs from the father and son of this family showed the classic features of pili torti under scanning electron microscopy.

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Year:  2002        PMID: 11807445     DOI: 10.1067/mjd.2002.107969

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  3 in total

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Journal:  J Dermatol Case Rep       Date:  2008-07-07

2.  Bjornstad syndrome.

Authors:  Deepa Aggarwal; Kabir Sardana; Praveen Kumar; Vivek Dewan; V K Anand
Journal:  Indian J Pediatr       Date:  2004-08       Impact factor: 1.967

3.  Cutaneous T-cell lymphoma in erythrodermic cases may be suspected on the basis of scalp examination with dermoscopy.

Authors:  Adriana Rakowska; Magdalena Jasińska; Mariusz Sikora; Joanna Czuwara; Patrycja Gajda-Mróz; Olga Warszawik-Hendzel; Małgorzata Kwiatkowska; Anna Waśkiel-Burnat; Małgorzata Olszewska; Lidia Rudnicka
Journal:  Sci Rep       Date:  2021-01-11       Impact factor: 4.379

  3 in total

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