Trisomy 9p, a Chromosome Aberration with Distinct Radiologic Findings
- 1 January 1979
- journal article
- research article
- Published by Radiological Society of North America (RSNA) in Radiology
- Vol. 130 (1) , 125-133
- https://doi.org/10.1148/130.1.125
Abstract
Radiographic analysis of 33 cases of trisomy 9p (21 familial, 12 nonfamilial) disclosed consistent abnormalities in the hands, feet and pelvic bones, with one exception (subsequently considered a misdiagnosis). Most of the abnormalities were present only during the period of epiphyseal growth and occurred with similar frequency in both familial and nonfamilial cases. There was no correlation between the severity of osseous involvement and the amount of trisomic chromosomal material. The pattern of radiographic findings in trisomy 9p appears to be unique, at least among chromosome aberrations, and may help in establishing a specific diagnosis in nonfamilial cases.This publication has 5 references indexed in Scilit:
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- Possible intrachromosomal duplication in a case of trisomy 9pHuman Genetics, 1976
- 9p trisomy identified by Giemsa-11Human Genetics, 1976
- 47,+(9q-) in unrelated three children with plasma growth hormon deficiencyHuman Genetics, 1976
- A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).Journal of Medical Genetics, 1975