Sanjad-Sakati syndrome in Al Najaf governorate

Author

al-Tahir, Mahir Muhammad Ali

Source

Kufa Medical Journal

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

Medicine

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