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Isolated rhomboencephalosynapsis : a rare cerebellar anomaly
rhomboencephalosynapsis
cerebellar malformation
children
Bibliogr. s. 49
Background: Rhomboencephalosynapsis (RES, RS) is a unique entity usually recognized in infancy based on neuroimaging. Cerebellar fusion and absence of cerebellar vermis is often associated with supratentorial findings. Since now there are about 50 cases described worldwide, with approximately 36 patients diagnosed by MRI. The authors present the first in Poland case of this uncommon malformation and review the literature. Case Report: The authors describe a 28-month-old-girl with microcephaly and proper psychomotor development. The family history was unrelevant. Based on MRI the congenital malformation of posterior fossarhombencephalosynapsis was confirmed Conclusions: Presented patient is a typical example of MRI usefulness especially in patients with RES. RES symptoms are mild and that is why the diagnosis is usually made only in adulthood.
| dc.abstract.en | Background: Rhomboencephalosynapsis (RES, RS) is a unique entity usually recognized in infancy based on neuroimaging. Cerebellar fusion and absence of cerebellar vermis is often associated with supratentorial findings. Since now there are about 50 cases described worldwide, with approximately 36 patients diagnosed by MRI. The authors present the first in Poland case of this uncommon malformation and review the literature. Case Report: The authors describe a 28-month-old-girl with microcephaly and proper psychomotor development. The family history was unrelevant. Based on MRI the congenital malformation of posterior fossarhombencephalosynapsis was confirmed Conclusions: Presented patient is a typical example of MRI usefulness especially in patients with RES. RES symptoms are mild and that is why the diagnosis is usually made only in adulthood. | pl |
| dc.contributor.author | Paprocka, Justyna | pl |
| dc.contributor.author | Jamroz, Ewa | pl |
| dc.contributor.author | Ścieszka, Ewa | pl |
| dc.contributor.author | Kluczewska, Ewa | pl |
| dc.date.accessioned | 2017-09-07T12:46:13Z | |
| dc.date.available | 2017-09-07T12:46:13Z | |
| dc.date.issued | 2012 | pl |
| dc.date.openaccess | 0 | |
| dc.description.accesstime | w momencie opublikowania | |
| dc.description.additional | Bibliogr. s. 49 | pl |
| dc.description.number | 1 | pl |
| dc.description.physical | 47-49 | pl |
| dc.description.version | ostateczna wersja wydawcy | |
| dc.description.volume | 77 | pl |
| dc.identifier.doi | 10.12659/PJR.882587 | pl |
| dc.identifier.eissn | 1899-0967 | pl |
| dc.identifier.issn | 1733-134X | pl |
| dc.identifier.uri | http://ruj.uj.edu.pl/xmlui/handle/item/43933 | |
| dc.language | eng | pl |
| dc.language.container | eng | pl |
| dc.rights | Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych 3.0 Polska | * |
| dc.rights.licence | CC-BY-NC-ND | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/pl/legalcode | * |
| dc.share.type | otwarte czasopismo | |
| dc.subject.en | rhomboencephalosynapsis | pl |
| dc.subject.en | cerebellar malformation | pl |
| dc.subject.en | children | pl |
| dc.subtype | Article | pl |
| dc.title | Isolated rhomboencephalosynapsis : a rare cerebellar anomaly | pl |
| dc.title.journal | Polish Journal of Radiology | pl |
| dc.type | JournalArticle | pl |
| dspace.entity.type | Publication |
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