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Hereditary benign intra-epithelial dyskeratosis (HBID) : (witkop-von sallman syndrome)
Joint Authors
al-Mahmud B.
al-Hayki N.
al-Musallamni H.
Source
Issue
Vol. 20, Issue 1 (30 Jun. 2011), pp.51-53, 3 p.
Publisher
Publication Date
2011-06-30
Country of Publication
Qatar
No. of Pages
3
Main Subjects
Topics
Abstract EN
Hereditary Benign Intraepithelial Dyskeratosis (HBID) is a rare autosomal dominant recurring disorder of the oral and ocular mucosa first described in 1960 among Haliwa Native American Indians in North Carolina.
A few cases have been reported also in other parts of the United States, South America and Europe.
This report describes a case with clinical and histopathologi-cal features of HBID.
American Psychological Association (APA)
al-Mahmud B.& al-Hayki N.& al-Musallamni H.. 2011. Hereditary benign intra-epithelial dyskeratosis (HBID) : (witkop-von sallman syndrome). Qatar Medical Journal،Vol. 20, no. 1, pp.51-53.
https://search.emarefa.net/detail/BIM-366271
Modern Language Association (MLA)
al-Mahmud B.…[et al.]. Hereditary benign intra-epithelial dyskeratosis (HBID) : (witkop-von sallman syndrome). Qatar Medical Journal Vol. 20, no. 1 (Jun. 2011), pp.51-53.
https://search.emarefa.net/detail/BIM-366271
American Medical Association (AMA)
al-Mahmud B.& al-Hayki N.& al-Musallamni H.. Hereditary benign intra-epithelial dyskeratosis (HBID) : (witkop-von sallman syndrome). Qatar Medical Journal. 2011. Vol. 20, no. 1, pp.51-53.
https://search.emarefa.net/detail/BIM-366271
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 53
Record ID
BIM-366271