Literature DB >> 15023374

Hereditary porencephaly: clinical and MRI findings in two Dutch families.

G M S Mancini1, I F M de Coo, M H Lequin, W F Arts.   

Abstract

Familial porencephaly is a rare disorder causing motor impairment, hemiplegia, mental retardation and epilepsy in variable degrees. Two families with porencephaly and apparently dominant inheritance are reported. Brain MRI findings are reviewed and described in seven affected individuals. Most patients also show white matter abnormalities in the cerebral hemisphere, also contralateral to the cystic lesion. In the first family an obligate carrier was identified who did not have a cystic lesion but clear abnormalities of the white matter. Although a predisposition for thrombophilia has previously been reported, we did not observe any genetic, environmental or epigenetic predisposition for the porencephaly. The lesions are most compatible with a deep venous thrombosis/ischemic event occurring in a late stage of pregnancy, not necessarily aggravated by perinatal asphyxia.

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Year:  2004        PMID: 15023374     DOI: 10.1016/j.ejpn.2003.10.002

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  6 in total

Review 1.  Genetic defects of human brain development.

Authors:  Jenny Carmichael; Christopher Woods
Journal:  Curr Neurol Neurosci Rep       Date:  2006-09       Impact factor: 5.081

2.  De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephaly.

Authors:  Yuriko Yoneda; Kazuhiro Haginoya; Hiroshi Arai; Shigeo Yamaoka; Yoshinori Tsurusaki; Hiroshi Doi; Noriko Miyake; Kenji Yokochi; Hitoshi Osaka; Mitsuhiro Kato; Naomichi Matsumoto; Hirotomo Saitsu
Journal:  Am J Hum Genet       Date:  2011-12-29       Impact factor: 11.025

3.  Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly.

Authors:  G Breedveld; I F de Coo; M H Lequin; W F M Arts; P Heutink; D B Gould; S W M John; B Oostra; G M S Mancini
Journal:  J Med Genet       Date:  2005-08-17       Impact factor: 6.318

4.  Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome.

Authors:  S Alamowitch; E Plaisier; P Favrole; C Prost; Z Chen; T Van Agtmael; B Marro; P Ronco
Journal:  Neurology       Date:  2009-12-01       Impact factor: 9.910

5.  COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.

Authors:  Cassandre Labelle-Dumais; David J Dilworth; Emily P Harrington; Michelle de Leau; David Lyons; Zhyldyz Kabaeva; M Chiara Manzini; William B Dobyns; Christopher A Walsh; Daniel E Michele; Douglas B Gould
Journal:  PLoS Genet       Date:  2011-05-19       Impact factor: 5.917

6.  Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.

Authors:  Sara Zagaglia; Christina Selch; Jelena Radic Nisevic; Davide Mei; Zuzanna Michalak; Laura Hernandez-Hernandez; S Krithika; Katharina Vezyroglou; Sophia M Varadkar; Alexander Pepler; Saskia Biskup; Miguel Leão; Jutta Gärtner; Andreas Merkenschlager; Michaela Jaksch; Rikke S Møller; Elena Gardella; Britta Schlott Kristiansen; Lars Kjærsgaard Hansen; Maria Stella Vari; Katherine L Helbig; Sonal Desai; Constance L Smith-Hicks; Naomi Hino-Fukuyo; Tiina Talvik; Rael Laugesaar; Pilvi Ilves; Katrin Õunap; Ingrid Körber; Till Hartlieb; Manfred Kudernatsch; Peter Winkler; Mareike Schimmel; Anette Hasse; Markus Knuf; Jan Heinemeyer; Christine Makowski; Sondhya Ghedia; Gopinath M Subramanian; Pasquale Striano; Rhys H Thomas; Caroline Micallef; Maria Thom; David J Werring; Gerhard Josef Kluger; J Helen Cross; Renzo Guerrini; Simona Balestrini; Sanjay M Sisodiya
Journal:  Neurology       Date:  2018-11-09       Impact factor: 9.910

  6 in total

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