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Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q

โœ Scribed by Cody, Jannine D.; Davis Ghidoni, Patricia; DuPont, Barbara R.; Hale, Daniel E.; Hilsenbeck, Susan G.; Stratton, Robert F.; Hoffman, Douglas S.; Muller, Shaine; Schaub, Rebecca L.; Leach, Robin J.; Kaye, Celia I.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
81 KB
Volume
85
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19990827)85:5<455::aid-ajmg5>3.0.co;2-z

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โœฆ Synopsis


Most deletions are terminal encompassing as much as 36 Mb, but interstitial deletions have also been reported. We have evaluated 42 subjects with deletions of 18q at our institution. This is the largest number of individuals with this chromosome abnormality studied by one group of investigators. Here we report the physical findings in these individuals. We have compared our findings with those of previously reported cases and have found a significantly different incidence of several minor anomalies in our subjects. We also describe here several anomalies not previously reported in individuals with deletions of 18q, including short frenulum, short palpebral fissures, disproportionate short stature, overlap of second and third toes, and a prominent abdominal venous pattern. Characteristics found in subjects were analyzed for correlation with cytogenetic breakpoints. Several traits were found to correlate with the extent of the deletion. Large deletions were associated with significantly decreased head circumference and ear length as well as the presence of proximally placed and/or anomalous thumbs. Individuals with the smallest deletions were more likely to have metatarsus adductus. Although relatively few genotype/phenotype correlations were apparent, these data demonstrate that correlations with breakpoint are possible. This implies that more correlations will become evident when the more precise molecularly based genotyping is completed. These correlations will identify critical regions on the chromosome in which genes responsible for specific abnormal phenotypes are located. Am.


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