A case of X-linked hypohidrotic ectodermal dysplasia (XHED) was identified in a family of Danish Red Holstein cattle. The ectodysplasin-signalling protein (EDA) is known to be central in the normal development of ectodermal structures, and mutations in the ectodysplasin A (EDA) gene have been reported to cause XHED. In this study, we analysed different EDA transcript variants in affected and unaffected cattle and identified a new transcript variant including a LINE1-derived pseudoexon between EDA exons 1 and 2. The 161-bp-long pseudoexon introduces a shift in reading frame and a premature stop codon early in EDA exon 2 and is probably the cause of XHED in this Danish Red Holstein family.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1111/j.1365-2052.2011.02192.x | DOI Listing |
Cureus
October 2024
Department of Dermatology, Naval Medical Center San Diego, San Diego, USA.
We report a case of a patient with genetic sequencing-confirmed X-linked hypohidrotic ectodermal dysplasia without the typical characteristic hair growth abnormalities with the disorder. While this patient had already received guidance from a genetic counselor about his condition, many cases of ectodermal dysplasia go underdiagnosed or misdiagnosed due to mild or atypical presentations. With gene therapies emerging, the authors hope to highlight the importance of recognizing the disorder in patients who have not yet received a diagnosis to better manage their clinical course and guide future life decisions.
View Article and Find Full Text PDFGenes (Basel)
June 2024
Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
Clin Cosmet Investig Dermatol
June 2024
Dermatological Department, The Affiliated Hospital of QingdaoUniversity, Qingdao, People's Republic of China.
Introduction: Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder that influences structures of ectodermal origin, such as teeth, hair, and sweat glands. Compared with autosomal recessive and dominant modes of inheritance, the X-linked HED (XLHED) characterized by Hypodontia/Oligodontia teeth, Absent/sparse hair, Anhidrosis/hypohidrosis, and characteristic facial features, is the most frequent and its primary cause is the mutation of ectodysplasin A (EDA) gene. This research aimed to expound the clinical and molecular features of a Chinese male with XLHED and to summarize and compare several previous findings.
View Article and Find Full Text PDFJAMA Dermatol
May 2024
Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!