A CASE REPORT OF A RARE FAMILIAL CAVERNOUS MALFORMATION IN HAMADAN FARSHCHIAN HOSPITAL

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GHIASIAN M.; MANSOUR M.

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Paper Information

Journal: JOURNAL OF ILAM UNIVERSITY OF MEDICAL SCIENCES Year:2016 | Volume:24 | Issue:5 Page(s): 42-47

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Title

A CASE REPORT OF A RARE FAMILIAL CAVERNOUS MALFORMATION IN HAMADAN FARSHCHIAN HOSPITAL

Author(s)

GHIASIAN M. | MANSOUR M. | Issue Writer Certificate

Keywords

CAVERNOUS MALFORMATIONQ1

AUTOSOMAL DOMINANTQ1

MAGNETIC RESONANCE IMAGINGQ2

Abstract

CAVERNOUS MALFORMATION is an abnormal vascular lesion caused by dysfunction in vessel wall. This disease is often asymptomatic but seizure, hemorrhage, progressive neurological deficit and headache may be seen. CAVERNOUS MALFORMATION usually presents as individual lesions. Multiple lesions are rare and can be familial with an AUTOSOMAL DOMINANT pattern. In this study a 41-year-old woman presenting with progressive neurological deficit consisting of diplopia, vertigo and facial palsy to hospital was examined and multiple CAVERNOUS MALFORMATION lesions were found. These lesions were also present in examination of other family members.

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APA: Copy

GHIASIAN, M., & MANSOUR, M.. (2016). A CASE REPORT OF A RARE FAMILIAL CAVERNOUS MALFORMATION IN HAMADAN FARSHCHIAN HOSPITAL. JOURNAL OF ILAM UNIVERSITY OF MEDICAL SCIENCES, 24(5), 42-47. SID. https://sid.ir/paper/90018/en

Vancouver: Copy

GHIASIAN M., MANSOUR M.. A CASE REPORT OF A RARE FAMILIAL CAVERNOUS MALFORMATION IN HAMADAN FARSHCHIAN HOSPITAL. JOURNAL OF ILAM UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2016;24(5):42-47. Available from: https://sid.ir/paper/90018/en

IEEE: Copy

M. GHIASIAN, and M. MANSOUR, “A CASE REPORT OF A RARE FAMILIAL CAVERNOUS MALFORMATION IN HAMADAN FARSHCHIAN HOSPITAL,” JOURNAL OF ILAM UNIVERSITY OF MEDICAL SCIENCES, vol. 24, no. 5, pp. 42–47, 2016, [Online]. Available: https://sid.ir/paper/90018/en

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