Dermatology Medical News about Ichthyosiform Erythroderma

Become a Member Today!
Register

Most Viewed Abstracts

1. Report Shows Shift in Starting Salaries for Physicians

2. 2008 Exclusive Survey—Earnings: Good news for primary care income

3. Medicare pay-for-reporting effort draws fire from frustrated doctors

4. Debunking Myths in the US Healthcare System

5. Doctors and the DEA Free full text

Your Article Summary

See Latest Articles

(Click the title below to leave the MDLinx Network and go to the Journal's Website)

Bullous Congenital Ichthyosiform Erythroderma: A Sporadic Case Produced by a New KRT10 Gene Mutation
Pediatric Dermatology, 08/14/09

Betlloch I et al. – The authors report the case of a girl with typical clinical and histopathologic findings of bullous congenital ichthyosiform erythroderma, who was found to have a new mutation in KRT10 gene, Glu445Lys at position 445, affecting the 2B region of the KRT10 protein, the end of the rod domain, where many other keratin mutations associated with hereditary skin disease have been reported.

<< Previous
Para-phenylenediamine and allergic sensitization: risk...

Next >>
Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP)...