Literature DB >> 1879585

Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.

P Calzavara-Pinton1, A Carlino, A Benetti, G De Panfilis.   

Abstract

Ectodermal dysplasias are a large and heterogeneous groups of clinically and genetically distinct syndromes. We studied a family suffering from dystrophies of the distal part of the nails and trichodysplasia. Scalp, beard, pubic and axillary hair were broken off leaving a stubble 1-10 mm in length. Eyebrows, eyelashes and body hair were completely absent. Serum levels of copper and plasma levels of amino acids were within the normal range. Inheritance was autosomal recessive. Previous reports of ectodermal dysplasias and other complex syndromes with pili torti are reviewed.

Entities:  

Mesh:

Year:  1991        PMID: 1879585

Source DB:  PubMed          Journal:  Dermatologica        ISSN: 0011-9075


  7 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.  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

5.  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

6.  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

7.  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

  7 in total

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