Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis

Sipahi, T; Uner, C; Yildiz, YT; Akar, N

doi:10.1007/s002470050776

Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis

Sipahi T., Uner C., Yildiz Y., Akar N.

PEDIATRIC RADIOLOGY, cilt.30, sa.6, ss.420-423, 2000 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 30 Sayı: 6
Basım Tarihi: 2000
Doi Numarası: 10.1007/s002470050776
Dergi Adı: PEDIATRIC RADIOLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.420-423
Ankara Üniversitesi Adresli: Hayır

Özet

Common systemic disorders that cause cerebral venous thrombosis (CVT) in children include dehydration, trauma, infection and haematological diseases. No cause for CVT is identified in one quarter of all cases. We report a child with thalamic infarcts due to internal CVT who had congenital heterozygous protein-C deficiency, factor V G 1691 Aand A 4070 G mutations.