Publications

Detailed Information

Lissencephaly and Mild Cerebellar Vermis Hypoplasia in a Case of Microcephaly and Chorioretinal Dysplasia

DC Field Value Language
dc.contributor.authorLee, Byung Joo-
dc.contributor.authorKim, Jeong Hun-
dc.contributor.authorYu, Young Suk-
dc.date.accessioned2012-06-29T01:04:51Z-
dc.date.available2012-06-29T01:04:51Z-
dc.date.issued2010-06-
dc.identifier.citationOPHTHALMIC GENETICS; Vol.31 2; 89-93ko_KR
dc.identifier.issn1381-6810-
dc.identifier.urihttps://hdl.handle.net/10371/77855-
dc.description.abstractPurpose: Microcephaly and chorioretinal dysplasia is a very rare syndrome, characterized by microcephaly, chorioretinal dysplasia, mental retardation, and is phenotypically classified according to the presence of lymphedema. Among previously described patients, there has been no association with brain anomaly other than simple microcephaly, except for one case that presented with micro-lissencephaly, who had lymphedema. Methods: Herein, we describe a case of microcephaly and chorioretinal dysplasia without lymphedema who was shown to have lissencephaly and cerebellar vermis hypoplasia. His head circumference at birth was 28 cm (below-3SD) and both fundi showed pigmentary retinopathy with multiple punched-out lesions and retinal vascular attenuation. Results: Magnetic resonance imaging of the brain showed lissencephaly accompanied by inferior cerebellar vermis hypoplasia. Conclusions: These results show that microcephaly and chorioretinal dysplasia can be accompanied by lissencepahly, thus brain imaging should be considered in evaluating these patients.ko_KR
dc.language.isoenko_KR
dc.publisherINFORMA HEALTHCAREko_KR
dc.subjectCerebellar vermis hypoplasiako_KR
dc.subjectChorioretinal dysplasiako_KR
dc.subjectMicrocephalyko_KR
dc.subjectLissencephalyko_KR
dc.subjectChorioretinopathyko_KR
dc.titleLissencephaly and Mild Cerebellar Vermis Hypoplasia in a Case of Microcephaly and Chorioretinal Dysplasiako_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor이병주-
dc.contributor.AlternativeAuthor김정훈-
dc.contributor.AlternativeAuthor유영석-
dc.identifier.doi10.3109/13816811003620509-
dc.citation.journaltitleOPHTHALMIC GENETICS-
dc.description.citedreferenceEventov-Friedman S, 2009, ACTA PAEDIATR, V98, P758, DOI 10.1111/j.1651-2227.2008.01161.x-
dc.description.citedreferenceAhmadi H, 2007, OPHTHALMIC GENET, V28, P210, DOI 10.1080/13816810701538554-
dc.description.citedreferenceTrzupek KM, 2007, AM J MED GENET A, V143A, P1218, DOI 10.1002/ajmg.a.31717-
dc.description.citedreferenceVerloes A, 2007, REV NEUROL-FRANCE, V163, P533-
dc.description.citedreferenceABUELO D, 2007, SEMIN PEDIAT NEUROL, V14, P118-
dc.description.citedreferenceForman MS, 2005, J NEUROPATH EXP NEUR, V64, P847-
dc.description.citedreferenceVasudevan PC, 2005, CLIN DYSMORPHOL, V14, P109-
dc.description.citedreferenceStrauss RM, 2005, PEDIATR DERMATOL, V22, P373-
dc.description.citedreferenceLeventer RJ, 2005, J CHILD NEUROL, V20, P307-
dc.description.citedreferenceNguyen TN, 2005, CAN J OPHTHALMOL, V40, P195-
dc.description.citedreferenceKato M, 2003, HUM MOL GENET, V12, pR89, DOI 10.1093/hmg/ddg086-
dc.description.citedreferenceSimonelli F, 2002, J PEDIAT OPHTH STRAB, V39, P288-
dc.description.citedreferenceBarkovich AJ, 2001, NEUROLOGY, V57, P2168-
dc.description.citedreferenceRoss ME, 2001, NEUROPEDIATRICS, V32, P256-
dc.description.citedreferenceMochida GH, 2001, CURR OPIN NEUROL, V14, P151-
dc.description.citedreferenceCasteels I, 2001, BRIT J OPHTHALMOL, V85, P499-
dc.description.citedreferenceAbdel-Salam GMH, 2000, AM J MED GENET, V95, P513-
dc.description.citedreferenceLimwongse C, 1999, AM J MED GENET, V86, P215-
dc.description.citedreferenceDobyns WB, 1999, NEUROLOGY, V53, P270-
dc.description.citedreferencevan Genderen MM, 1997, OPHTHALMIC GENET, V18, P199-
dc.description.citedreferenceKozma C, 1996, CLIN DYSMORPHOL, V5, P49-
dc.description.citedreferenceHordijk R, 1996, GENET COUNSEL, V7, P113-
dc.description.citedreferenceFRYNS JP, 1995, CLIN GENET, V48, P131-
dc.description.citedreferenceANGLE B, 1994, AM J MED GENET, V53, P99-
dc.description.citedreferenceWARBURG M, 1994, AM J MED GENET, V52, P117-
dc.description.citedreferenceSADLER LS, 1993, AM J MED GENET, V47, P65-
dc.description.citedreferenceFEINGOLD M, 1992, AM J MED GENET, V43, P1030-
dc.description.citedreferenceMANNING FJ, 1990, AM J OPHTHALMOL, V109, P457-
dc.description.citedreferenceYOUNG ID, 1987, J MED GENET, V24, P172-
dc.description.citedreferenceMENDEZ HMM, 1985, AM J MED GENET, V22, P223-
dc.description.citedreferencePARKE JT, 1984, AM J MED GENET, V17, P585-
dc.description.citedreferenceJARMAS AL, 1981, AM J DIS CHILD, V135, P930-
dc.description.citedreferenceTENCONI R, 1981, CLIN GENET, V20, P347-
dc.description.citedreferenceCANTU JM, 1977, HUM GENET, V36, P243-
dc.description.citedreferenceMIRHOSSEINI SA, 1972, J MED GENET, V9, P193-
dc.description.citedreferenceMCKUSICK VA, 1966, ARCH OPHTHALMOL-CHIC, V75, P597-
dc.description.tc0-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share