We describe a patient with microcephaly, developmental delay, and nephrotic syndrome who had normal renal function and normal brain imaging studies. She does not have the Galloway-Mowat syndrome. The concurrence of nephrotic syndrome with microcephaly and developmental delay may be coincidental, or
No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome
โ Scribed by Marinescu, R. Catrinel; Johnson, Elizabeth I.; Dykens, Elisabeth M.; Hodapp, Robert M.; Overhauser, Joan
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 28 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19990903)86:1<66::aid-ajmg13>3.0.co;2-n
No coin nor oath required. For personal study only.
โฆ Synopsis
Molecular cytogenetic and developmental assessment was performed on 50 individuals with cri-du-chat syndrome. Fluorescent in situ hybridization analysis was used to confirm a terminal deletion karyotype and map more precisely the location of the deletion breakpoint. We identified terminal deletion breakpoints mapping from 5p15.2 to 5p13. Developmental assessment was performed using the Vineland Adaptive Behavior Scales test. Composite Vineland Scores ranged from 20-75. In general, the communication score was higher than the composite score. Comparison of the size of the deletion with the composite Vineland score, as well as the Vineland Communication score, demonstrated that there was no correlation between the size of the deletion and the level of developmental delay. These results demonstrate that patients with cri-du-chat syndrome show high variability in the level of developmental achievement. Am. J. Med. Genet. 86:66-70, 1999.
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