Hereditary benign intra-epithelial dyskeratosis (HBID)‎ : (witkop-von sallman syndrome)‎

Joint Authors

al-Mahmud B.
al-Hayki N.
al-Musallamni H.

Source

Qatar Medical Journal

Issue

Vol. 20, Issue 1 (30 Jun. 2011), pp.51-53, 3 p.

Publisher

Hamad Medical Corporation

Publication Date

2011-06-30

Country of Publication

Qatar

No. of Pages

3

Main Subjects

Medicine

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