Report of three rare cases of Dowling Dego's disease
Dowling Dego's disease is a rare autosomal dominant condition. It is caused by loss of function mutations in keratin 5 gene (kRT5) situated in keratin gene cluster on 12q13. We are reporting three cases of Dowling Dego's disease out of which two belong to same family. The clinical manifest...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Deccan College of Medical Sciences
2017-07-01
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| Series: | Journal of Medical and Allied Sciences |
| Subjects: | |
| Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=260932 |