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| Title: | Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8. |
| Author(s): | Feenstra, I. (321517369) Ravenswaaij-Arts, C.M.A. van (230344143) Knaap, M.S. van der Willemsen, M.A.A.P. (23476452X) |
| Publication year: | 2006 |
| Document type: | Article / Letter to editor |
| Journal: | Neuropediatrics |
| ISSN: | 0174-304X |
| Volume: | vol. 37 |
| Issue: | iss. 2 |
| Start page: | p. 83 |
| End page: | p. 87 |
| Abstract: | Inversion duplication 8p is a rare chromosome disorder characterised by severe mental retardation, minor facial dysmorphisms, and corpus callosum agenesis. Few cerebral imaging studies have been reported. We describe 9 patients with an inversion duplication 8p, involving variable segments of the short arm of chromosome 8. MRI was performed in 8 patients and 2 patients underwent CT scanning. The images were systematically reviewed. All patients suffered from severe mental retardation. Head circumference was between 0 and + 2 SD in 7 patients. The corpus callosum was absent in 6, and thin (but complete) in 3 patients. Hypoplasia of the (inferior) cerebellar vermis was observed in 6 patients. Enlargement of the ventricular system and associated hippocampal maldevelopment were found in all patients. The supratentorial external CSF spaces were enlarged in 6 patients, and in 3 patients there was a remarkable enlargement of the retrocerebellar arachnoidal space. Cerebral white matter showed mildly delayed myelination in 7 patients, and periventricular lesions of variable extent in 6 patients. The pattern of imaging abnormalities was non-specific, but remarkably similar between patients. We found no correlation between the severity of the clinical features, imaging results, and extent of the chromosomal aberration. |
| Subject: | UMCN 3.1: Neuromuscular development and genetic disorders UMCN 5.1: Genetic defects of metabolism |
| Organization: | Human Genetics UMCN Extern Paediatrics |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/50319
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