Literature DB >> 8733465

Persistent nasal crusting due to hypohidrotic ectodermal dysplasia.

A H Al-Jassim1, A C Swift.   

Abstract

Hypohidrotic ectodermal dysplasia is an hereditary condition of the ectodermal tissues which may escape recognition because of lack of clinical awareness due to its rarity. Otorhinolaryngological features of this syndrome include chronic respiratory tract infections, persistent foul-smelling nasal discharge and crust formation, and hearing problems. The condition is usually an X-linked recessive disease affecting mainly ectodermal tissue, although nonectodermal tissue may also be affected. The notation 'ectodermal' is used because ectodermal tissues are always involved. The syndrome is characterized by complete or partial absence of sweat glands, sparse hair growth, absent or deformed peg teeth, sparse sebaceous glands, occasional absence of salivary and lacrimal glands, scanty mucous glands and deficient cilia. We describe two children with this disorder with specific reference to the effect on the upper respiratory tract.

Entities:  

Mesh:

Year:  1996        PMID: 8733465     DOI: 10.1017/s0022215100133687

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  6 in total

1.  Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements.

Authors:  Sigrun Wohlfart; Johanna Hammersen; Holm Schneider
Journal:  J Hum Genet       Date:  2016-06-16       Impact factor: 3.172

2.  Neonatal treatment with recombinant ectodysplasin prevents respiratory disease in dogs with X-linked ectodermal dysplasia.

Authors:  Elizabeth A Mauldin; Olivier Gaide; Pascal Schneider; Margret L Casal
Journal:  Am J Med Genet A       Date:  2009-09       Impact factor: 2.802

3.  TRAF6-deficient mice display hypohidrotic ectodermal dysplasia.

Authors:  Asuka Naito; Hisahiro Yoshida; Eri Nishioka; Mizuho Satoh; Sakura Azuma; Tadashi Yamamoto; Shin-ichi Nishikawa; Jun-ichiro Inoue
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

4.  FGF and EDA pathways control initiation and branching of distinct subsets of developing nasal glands.

Authors:  Alison J May; Denis Headon; David P Rice; Alistair Noble; Abigail S Tucker
Journal:  Dev Biol       Date:  2016-08-30       Impact factor: 3.582

5.  Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.

Authors:  Sigrun Wohlfart; Ralph Meiller; Johanna Hammersen; Jung Park; Johannes Menzel-Severing; Volker O Melichar; Kenneth Huttner; Ramsey Johnson; Florence Porte; Holm Schneider
Journal:  Orphanet J Rare Dis       Date:  2020-01-10       Impact factor: 4.123

6.  No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.

Authors:  Laura Körber; Holm Schneider; Nicole Fleischer; Sigrun Maier-Wohlfart
Journal:  Orphanet J Rare Dis       Date:  2021-02-23       Impact factor: 4.123

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.