| Bilateral, perisylvian and rolandic cortical dysplasia in trisomy 13 syndrome. | |
| | |
MedLine Citation:
|
PMID: 9107109 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
In patients with the trisomy 13 syndrome the most commonly encountered brain anomaly is holoprosencephaly, which occurs in approximately 80% of cases. In trisomy 13 patients without holoprosencephaly, previously reported anomalies include callosal dysgenesis, hippocampal hypoplasia, olfactory hypoplasia, and cerebellar dysplastic changes such as vermian hypoplasia and dysplastic cortices. Dysplasia of the cerebral cortex, however, has not been reported before. We describe a newborn with bilateral, dysplastic cortices at the perisylvian and rolandic regions. These dysplastic cortices probably accounted for the clinical findings of seizures, oromotor dysfunction, dystonia flexion contractures in the hands, which were consistent with a recently described syndrome labelled as the "congenital bilateral perisylvian syndrome". |
| | |
Authors:
|
R N Sener |
Related Documents
:
|
15581839 - Partial trisomy 8q and partial monosomy 18p: a case report. 18022449 - Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: vacterl ... 6967279 - Partial trisomy 8 mosaicism with 46,xx/46,xx-8,+dic(8). 3732319 - Bronze baby syndrome, biliary hypoplasia, incomplete beckwith-wiedemann syndrome and pa... 174849 - Triploidy syndrome. a report on two live-born (69, xxy) and one still-born (69, xxx) in... 18798309 - Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes. |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Journal of neuroradiology. Journal de neuroradiologie Volume: 23 ISSN: 0150-9861 ISO Abbreviation: J Neuroradiol Publication Date: 1996 Dec |
Date Detail:
|
Created Date: 1997-05-20 Completed Date: 1997-05-20 Revised Date: 2008-02-20 |
Medline Journal Info:
|
Nlm Unique ID: 7705086 Medline TA: J Neuroradiol Country: FRANCE |
Other Details:
|
Languages: eng Pagination: 231-3 Citation Subset: IM |
Affiliation:
|
Department of Radiology, Ege University Hospital, Bornova, Izmir, Turkey. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Cerebellum
/
abnormalities Chromosomes, Human, Pair 13 / genetics* Contracture / etiology Corpus Callosum / abnormalities Dystonia / etiology Frontal Lobe / abnormalities* Hand Hippocampus / abnormalities Holoprosencephaly / diagnosis, pathology Humans Infant, Newborn Infant, Premature Male Mouth Diseases / etiology Movement Disorders / etiology Olfactory Pathways / abnormalities Seizures / etiology Syndrome Temporal Lobe / abnormalities* Trisomy / diagnosis*, pathology |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Magnetic resonance imaging using FLAIR pulse sequence in white matter diseases.
Next Document: Tuberculous radiculomyelitis as a complication of spondilodiscitis: MR demonstration.