Study of serum copper and ceruloplasmin levels in Egyptian autistic children

المؤلفون المشاركون

Muafi, Muhammad E.
Lutfi, Ahmad
al-Baz, Faridah

المصدر

The Egyptian Journal of Medical Human Genetics

العدد

المجلد 19، العدد 2 (30 إبريل/نيسان 2018)، ص ص. 113-116، 4ص.

الناشر

الجمعية المصرية للأمراض الوراثية

تاريخ النشر

2018-04-30

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

Background: Autism is a behaviorally defined neurodevelopmental disorder of unknown etiology.

Objective: To assess serum copper and ceruloplasmin levels in Egyptian autistic children patients.

Subjects and methods: 40 participants have been subjected to thorough history taking, complete clinical examination, IQ assessment, estimation of serum copper and ceruloplasmin levels.

Results: A statistically significant difference was found between patients and controls as regards stereotypic movements, absent eye contact, delayed motor development, delayed speech and IQ (p < 0.01 for each item).

Mean level of copper was significantly higher in patients than in controls (P < 0.001), also mean level of ceruloplasmin was significantly higher in patients than controls (P = 0.009).

Conclusion: Serum copper level may have a role in the pathogenesis of autism

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Baz, Faridah& Muafi, Muhammad E.& Lutfi, Ahmad. 2018. Study of serum copper and ceruloplasmin levels in Egyptian autistic children. The Egyptian Journal of Medical Human Genetics،Vol. 19, no. 2, pp.113-116.
https://search.emarefa.net/detail/BIM-902283

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Baz, Faridah…[et al.]. Study of serum copper and ceruloplasmin levels in Egyptian autistic children. The Egyptian Journal of Medical Human Genetics Vol. 19, no. 2 (Apr. 2018), pp.113-116.
https://search.emarefa.net/detail/BIM-902283

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Baz, Faridah& Muafi, Muhammad E.& Lutfi, Ahmad. Study of serum copper and ceruloplasmin levels in Egyptian autistic children. The Egyptian Journal of Medical Human Genetics. 2018. Vol. 19, no. 2, pp.113-116.
https://search.emarefa.net/detail/BIM-902283

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 116

رقم السجل

BIM-902283