Literature DB >> 9295083

Family with "pure" hair-nail ectodermal dysplasia.

M Barbareschi1, S Cambiaghi, A C Crupi, G Tadini.   

Abstract

"Pure" ectodermal dysplasias are developmental disorders affecting only tissues of ectodermal origin. Two different pure ectodermal dysplasias involving only hair and nails have been described to date. Here we describe congenital nail dystrophy and hypotrichosis associated with folliculitis decalvans in a family suggesting autosomal-dominant transmission. This report documents peculiar clinical and ultrastructural hair findings that fit poorly into previously described conditions. Thus the reported patients could represent a new type of pure ectodermal dysplasia.

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Year:  1997        PMID: 9295083     DOI: 10.1002/(sici)1096-8628(19971003)72:1<91::aid-ajmg19>3.0.co;2-p

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

Review 1.  [Genetic hair diseases. An update].

Authors:  J Frank; P Poblete-Gutiérrez; K Giehl
Journal:  Hautarzt       Date:  2013-11       Impact factor: 0.751

2.  Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.

Authors:  M Naeem; M Jelani; K Lee; G Ali; M S Chishti; A Wali; A Gul; P John; M J Hassan; S M Leal; W Ahmad
Journal:  Br J Dermatol       Date:  2006-12       Impact factor: 9.302

3.  Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.

Authors:  Zhimiao Lin; Quan Chen; Lei Shi; Mingyang Lee; Kathrin A Giehl; Zhanli Tang; Huijun Wang; Jie Zhang; Jinghua Yin; Lingshen Wu; Ruo Xiao; Xuanzhu Liu; Lanlan Dai; Xuejun Zhu; Ruoyu Li; Regina C Betz; Xue Zhang; Yong Yang
Journal:  Am J Hum Genet       Date:  2012-10-11       Impact factor: 11.025

4.  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

5.  A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.

Authors:  M Naeem; M Wajid; K Lee; S M Leal; W Ahmad
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318

6.  Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics.

Authors:  Anna Kutkowska-Kaźmierczak; Katarzyna Niepokój; Katarzyna Wertheim-Tysarowska; Aleksandra Giza; Maria Mordasewicz-Goliszewska; Jerzy Bal; Ewa Obersztyn
Journal:  J Appl Genet       Date:  2015-01-10       Impact factor: 3.240

7.  Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis.

Authors:  Doroteya Raykova; Joakim Klar; Aysha Azhar; Tahir Naeem Khan; Naveed Altaf Malik; Muhammad Iqbal; Muhammad Tariq; Shahid Mahmood Baig; Niklas Dahl
Journal:  PLoS One       Date:  2014-04-08       Impact factor: 3.240

8.  A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family.

Authors:  Anwar Kamal Khan; Noor Muhammad; Abdul Aziz; Sher Alam Khan; Khadim Shah; Abdul Nasir; Muzammil Ahmad Khan; Saadullah Khan
Journal:  BMC Med Genet       Date:  2017-04-12       Impact factor: 2.103

  8 in total

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