Study of serum copper and ceruloplasmin levels in Egyptian autistic children

Joint Authors

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

Source

The Egyptian Journal of Medical Human Genetics

Issue

Vol. 19, Issue 2 (30 Apr. 2018), pp.113-116, 4 p.

Publisher

Egyptian Society of Human Genetics

Publication Date

2018-04-30

Country of Publication

Egypt

No. of Pages

4

Main Subjects

Medicine

Abstract 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

American Psychological Association (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

Modern Language Association (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

American Medical Association (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

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references : p. 116

Record ID

BIM-902283