Sudanese infant with fraser syndrome
Other Title(s)
متلازمة فرايزر في طفل رضيع سوداني
Joint Authors
Yasin, Amir
al-Asad, Sumayyah
Abd al-Munim, Sawsan
Hashim, Amani
Hasan, Awad Allah
Source
Sudan Journal of Medical Sciences
Issue
Vol. 5, Issue 4 (31 Dec. 2010), pp.303-306, 4 p.
Publisher
Omdurman Islamic University Faculty of Medicine
Publication Date
2010-12-31
Country of Publication
Sudan
No. of Pages
4
Main Subjects
Topics
Abstract AR
متلازمة فرايزر هي من الأمراض ذات الصفة المتنحية تتميز بوجود اختباء العين و ارتفاق جلدي و تشوه قحفي وجهي مع تشوه في الممرات التنفسية العليا و القناة البولية التناسلية.
تشخيص متلازمة فرايزر مبني على الأعراض و العلامات السريرية.
هنا نقدم حالة طفل رضيع سوداني تم معاينته في مستشفى الطوارئ للأطفال بأم درمان.
Abstract EN
We are reporting here a case of Fraser syndrome which is a very rare autosomal recessive disorder characterized by cryptophthalmos, cutaneous syndactyly, craniofacial dysmorphism, malformation of the upper airways and genitourinary tract.
Diagnosis of Fraser syndrome is based on clinical signs.
American Psychological Association (APA)
Yasin, Amir& al-Asad, Sumayyah& Abd al-Munim, Sawsan& Hashim, Amani& Hasan, Awad Allah. 2010. Sudanese infant with fraser syndrome. Sudan Journal of Medical Sciences،Vol. 5, no. 4, pp.303-306.
https://search.emarefa.net/detail/BIM-292717
Modern Language Association (MLA)
Yasin, Amir…[et al.]. Sudanese infant with fraser syndrome. Sudan Journal of Medical Sciences Vol. 5, no. 4 (Dec. 2010), pp.303-306.
https://search.emarefa.net/detail/BIM-292717
American Medical Association (AMA)
Yasin, Amir& al-Asad, Sumayyah& Abd al-Munim, Sawsan& Hashim, Amani& Hasan, Awad Allah. Sudanese infant with fraser syndrome. Sudan Journal of Medical Sciences. 2010. Vol. 5, no. 4, pp.303-306.
https://search.emarefa.net/detail/BIM-292717
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 305
Record ID
BIM-292717
