MOEBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT

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ASHRAFI M.R.; HUSSAIN I.; ZAMANI S.M.A.

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Journal Paper

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Journal: ACTA MEDICA IRANICA Year:2006 | Volume:44 | Issue:6 Page(s): 432-434

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Information Journal Paper

Title

MOEBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT

Author(s)

ASHRAFI M.R. | HUSSAIN I. | ZAMANI S.M.A. | Issue Writer Certificate

Keywords

MOEBIUS SYNDROME

CORPUS CALLOSUM AGENESIS

THE STRAIGHTENING OF FOURTH VENTRICLE FLOOR

Abstract

MOEBIUS SYNDROME is a rare congenital disorder of the facial and abducens nerve. Other cranial nerves may be involved, such as V, IX and XII. Several central nervous system anomalies including hypoplastic or dysplastic brain stem, straightening of the fourth ventricle floor, focal necrosis and calcifications of cranial nerve nuclei have been reported in association with MOEBIUS SYNDROME, but we report a 18 months old boy of MOEBIUS SYNDROME with CORPUS CALLOSUM AGENESIS that has not been reported yet.

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APA: Copy

ASHRAFI, M.R., HUSSAIN, I., & ZAMANI, S.M.A.. (2006). MOEBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT. ACTA MEDICA IRANICA, 44(6), 432-434. SID. https://sid.ir/paper/277954/en

Vancouver: Copy

ASHRAFI M.R., HUSSAIN I., ZAMANI S.M.A.. MOEBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT. ACTA MEDICA IRANICA[Internet]. 2006;44(6):432-434. Available from: https://sid.ir/paper/277954/en

IEEE: Copy

M.R. ASHRAFI, I. HUSSAIN, and S.M.A. ZAMANI, “MOEBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT,” ACTA MEDICA IRANICA, vol. 44, no. 6, pp. 432–434, 2006, [Online]. Available: https://sid.ir/paper/277954/en

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