%0 Journal Article %1 Harum1999a %A Harum, K. H. %A Hoon, A. H. %A Kato, G. J. %A Casella, J. F. %A Breiter, S. N. %A Johnston, M. V. %D 1999 %J Dev Med Child Neurol %K Aortic Diseases; Cerebral Palsy; Child, Preschool; Coronary Thrombosis; Factor V; Female; Homozygote; Humans; Infant, Newborn; Leukomalacia, Periventricular; Magnetic Resonance Imaging; Point Mutation; Polymerase Chain Reaction %N 11 %P 777--780 %T Homozygous factor-V mutation as a genetic cause of perinatal thrombosis and cerebral palsy. %V 41 %X A 5-year old girl with cerebral palsy (CP), preterm birth, postnatal aortic thrombus, and cerebellar venous infarction who is homozygous for the thrombophilic factor-V Leiden (fVL) mutation is reported. The role of hereditary thrombophilic disorders in the development of perinatal vascular lesions such as aortic thrombi, renal-vein thrombosis, venous-sinus thrombosis, and cerebral infarction is unknown. This case report brings into question a potential association between fVL, perinatal vascular lesions, perinatal stroke, and CP.

@article{Harum1999a, abstract = {A 5-year old girl with cerebral palsy (CP), preterm birth, postnatal aortic thrombus, and cerebellar venous infarction who is homozygous for the thrombophilic factor-V Leiden (fVL) mutation is reported. The role of hereditary thrombophilic disorders in the development of perinatal vascular lesions such as aortic thrombi, renal-vein thrombosis, venous-sinus thrombosis, and cerebral infarction is unknown. This case report brings into question a potential association between fVL, perinatal vascular lesions, perinatal stroke, and CP.}, added-at = {2014-07-19T20:25:29.000+0200}, author = {Harum, K. H. and Hoon, A. H. and Kato, G. J. and Casella, J. F. and Breiter, S. N. and Johnston, M. V.}, biburl = {https://www.bibsonomy.org/bibtex/2ddbae740324061395bf3c4ebb81c7fe9/ar0berts}, groups = {public}, interhash = {a207d821a41d5fd48582e06853e569cb}, intrahash = {ddbae740324061395bf3c4ebb81c7fe9}, journal = {Dev Med Child Neurol}, keywords = {Aortic Diseases; Cerebral Palsy; Child, Preschool; Coronary Thrombosis; Factor V; Female; Homozygote; Humans; Infant, Newborn; Leukomalacia, Periventricular; Magnetic Resonance Imaging; Point Mutation; Polymerase Chain Reaction}, month = Nov, number = 11, pages = {777--780}, pmid = {10576642}, timestamp = {2014-07-19T20:25:29.000+0200}, title = {Homozygous factor-V mutation as a genetic cause of perinatal thrombosis and cerebral palsy.}, username = {ar0berts}, volume = 41, year = 1999 }