Sanjad-Sakati syndrome in Al Najaf governorate
Author
Source
Issue
Vol. 18, Issue 2 (31 Dec. 2022), pp.45-49, 5 p.
Publisher
University of Kufa Faculty of Medicine
Publication Date
2022-12-31
Country of Publication
Iraq
No. of Pages
5
Main Subjects
Abstract EN
Sanjad-Sakati syndrome is an inherited autosomal recessive disorder that presents primarily in the Arab countries, with its real prevalence not well established.
It is a combination of specific facial dysmorphology, failure to thrive, hypoparathyroidism, and variable mental disability which is an unfortunately incurable disease with fatal outcomes.
American Psychological Association (APA)
al-Tahir, Mahir Muhammad Ali. 2022. Sanjad-Sakati syndrome in Al Najaf governorate. Kufa Medical Journal،Vol. 18, no. 2, pp.45-49.
https://search.emarefa.net/detail/BIM-1494074
Modern Language Association (MLA)
al-Tahir, Mahir Muhammad Ali. Sanjad-Sakati syndrome in Al Najaf governorate. Kufa Medical Journal Vol. 18, no. 2 (Dec. 2022), pp.45-49.
https://search.emarefa.net/detail/BIM-1494074
American Medical Association (AMA)
al-Tahir, Mahir Muhammad Ali. Sanjad-Sakati syndrome in Al Najaf governorate. Kufa Medical Journal. 2022. Vol. 18, no. 2, pp.45-49.
https://search.emarefa.net/detail/BIM-1494074
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 49
Record ID
BIM-1494074