Literature DB >> 16427989

Hereditary woolly hair and keratosis pilaris.

Andy J Chien1, Mark C Valentine, Virginia P Sybert.   

Abstract

We describe a family with woolly hair and ulerythema ophryogenes spanning four generations. Both woolly hair and ulerythema ophryogenes have been associated with Noonan syndrome and cardiofaciocutaneous syndrome (CFC), two disorders with considerable phenotypic overlap. This family did not exhibit any of the other findings characteristic of either Noonan syndrome or CFC, similar to a previously described pedigree with hereditary woolly hair. Woolly hair elicits a broad differential diagnosis, including woolly hair nevus and several genodermatoses. Our report reviews the evaluation of woolly hair and discusses the conditions associated with this physical finding.

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Year:  2006        PMID: 16427989     DOI: 10.1016/j.jaad.2005.01.092

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


  11 in total

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Authors:  Adriana Rakowska; Monika Slowinska; Elzbieta Kowalska-Oledzka; Lidia Rudnicka
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2.  Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.

Authors:  Yutaka Shimomura; Maria C Garzon; Leonard Kristal; Lawrence Shapiro; Angela M Christiano
Journal:  Exp Dermatol       Date:  2008-09-18       Impact factor: 3.960

3.  Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.

Authors:  Yutaka Shimomura; Muhammad Wajid; Lynn Petukhova; Mazen Kurban; Angela M Christiano
Journal:  Am J Hum Genet       Date:  2010-03-25       Impact factor: 11.025

4.  Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis.

Authors:  M Kurban; M Wajid; Y Shimomura; A M Christiano
Journal:  J Eur Acad Dermatol Venereol       Date:  2012-03-05       Impact factor: 6.166

5.  Dsp rul: a spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome.

Authors:  C Herbert Pratt; Christopher S Potter; Heather Fairfield; Laura G Reinholdt; David E Bergstrom; Belinda S Harris; Ian Greenstein; Soheil S Dadras; Bruce T Liang; Paul N Schofield; John P Sundberg
Journal:  Exp Mol Pathol       Date:  2015-02-07       Impact factor: 3.362

6.  Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis.

Authors:  Yutaka Shimomura; Muhammad Wajid; Abraham Zlotogorski; Young-Jin Lee; Robert H Rice; Angela M Christiano
Journal:  J Invest Dermatol       Date:  2009-03-05       Impact factor: 8.551

7.  The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g.

Authors:  Legairre A Radden; Kevin M Child; Elisabeth B Adkins; Damek V Spacek; Aaron M Feliciano; Thomas R King
Journal:  BMC Res Notes       Date:  2013-05-09

8.  To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed.

Authors:  Barbara Gandolfi; Hasan Alhaddad; Verena K Affolter; Jeffrey Brockman; Jens Haggstrom; Shannon E K Joslin; Amanda L Koehne; James C Mullikin; Catherine A Outerbridge; Wesley C Warren; Leslie A Lyons
Journal:  PLoS One       Date:  2013-06-27       Impact factor: 3.240

9.  Familial woolly hair: a rare entity.

Authors:  Satyendra Kumar Singh; Kajal Manchanda; Anand Kumar; Anurag Verma
Journal:  Int J Trichology       Date:  2012-10

10.  An unusual case of korean brother and sister with woolly hair.

Authors:  Seung Il Choi; Sung Yul Lee
Journal:  Ann Dermatol       Date:  2012-11-08       Impact factor: 1.444

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