CONGENITAL FACIAL NERVE PARALYSIS

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

MALEKI M.S.; KHORAMINEZHAD S.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Razi Journal of Medical Sciences Year:2001 | Volume:7 | Issue:22 Page(s): 316-322

Download Full-Text

Persian Verion

View:

3,916

Download:

Cites:

Information Journal Paper

Title

CONGENITAL FACIAL NERVE PARALYSIS

Author(s)

MALEKI M.S. | KHORAMINEZHAD S. | Issue Writer Certificate

Keywords

CONGENITAL PARALYSIS OF FACIAL NERVEQ4

MOBIUS SYNDROMEQ4

Abstract

Mc Hugh has reported that incidence of neonatal facial nerve Paralysis in 1969, has been 0.23%. Infantile facial nerve paralysis has been categorized to three groups: 1- Congenital (Developmental) facial nerve paralysis2- Prenatal acquired facial nerve paralysis.3- Postnatal acquired facial nerve paralysisThe MOBIUS SYNDROME may be the most famous among the causes of congenital facial nerve paralysis. Many suggest the vascular theory for Mobius syrdome. This syndrome has a wide range of clinic pathological signs and symptoms from unilateral facial nerve paralysis to bilateral Facial and Cranial nerve VI paralysis.The involvement of other cranial nerves (IX, X, XII) also has been reported. Few reports suggest the autosomal dominant inheritance of this syndrome and few families presented which several of their members in different generation were disabled with this syndrome. In our research of the literature, we did not found any report about two siblings who are affected by this syndrome. In our cases, family history was negative. Their mother has no history of thalidomide or misoprostol use or rubella during preganacy. The first case is an 18 - year - old male and his right facial nerve is paralyzed. His EMG and NCV show no response in right side. In his temporal bone CT scan, the mastoidian segment of right facial nerve is narrower than contralateral side. The second case is a 16.5 - year - old female and her left facial nerve is paretic. She has been operated for her strabismus when she was 9 - year - old. Her EMG and NCV shows decreased response in left side. In her temporal bone CT scan, the mastoidan segment of left facial nerve is narrower than right side.

Cites

No record.

References

No record.

Cite

APA: Copy

MALEKI, M.S., & KHORAMINEZHAD, S.. (2001). CONGENITAL FACIAL NERVE PARALYSIS. RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES), 7(22), 316-322. SID. https://sid.ir/paper/10024/en

Vancouver: Copy

MALEKI M.S., KHORAMINEZHAD S.. CONGENITAL FACIAL NERVE PARALYSIS. RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES)[Internet]. 2001;7(22):316-322. Available from: https://sid.ir/paper/10024/en

IEEE: Copy

M.S. MALEKI, and S. KHORAMINEZHAD, “CONGENITAL FACIAL NERVE PARALYSIS,” RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES), vol. 7, no. 22, pp. 316–322, 2001, [Online]. Available: https://sid.ir/paper/10024/en

Related Journal Papers