๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Multiple meningiomas in a patient with constitutional ring chromosome 22

โœ Scribed by Petrella, Rena ;Levine, Seymour ;Wilmot, Patrick L. ;Ashar, Kunjlata D. ;Casamassima, Anthony C. ;Shapiro, Lawrence R.


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
360 KB
Volume
47
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

โœฆ Synopsis


We report on a patient with multiple congenital anomalies and ring chromosome 22 who died at age 16 years of bronchopneumonia. Autopsy documented multiple psammomatous meningiomas of the spinal dura and tentorium. n m o r tissue for cytogenetic analysis was not available. Although abnormalities of chromosome 22 in tumor tissue have been reported, to our knowledge, this is only the third report of a constitutional chromosome 22 abnormality associated with the development of meningiomas. Thus, a constitutional chromosome 22 abnormality may predispose to the development of meningiomas.


๐Ÿ“œ SIMILAR VOLUMES


Ring chromosome 22 karyotype in a patien
โœ Christodoulou, John ;Bankier, Agnes ;Loughnan, Peter ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 257 KB ๐Ÿ‘ 2 views

## To the Editor: The Opitz or BBBG syndrome is an autosomal dominant disorder characterized by facial anomalies and multiple congenital abnormalities. Recent evidence would suggest that the Opitz and BBB syndromes form a spectrum of the same condition Verloes et al., 19891 and it has been sugges

Occipital lobe meningioma in a patient w
โœ Joel F. Moorhead; Anthony J. Suruda ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 138 KB ๐Ÿ‘ 1 views

Background The concurrent diagnosis of meningioma with increased intracranial pressure has not been reported previously in a patient who meets diagnostic criteria for multiple chemical sensitivities (MCS). Methods A patient who had been evaluated in an occupational medicine practice, and by several

Constitutional ring chromosome 11 mosaic
โœ Massimo Carella; Filippo Spreafico; Orazio Palumbo; Clelia Tiziana Storlazzi; Si ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 212 KB ๐Ÿ‘ 2 views

## Abstract We report on a boy with three cell lines: 46,XY, r(11)(p15.5,q25)[90]/45,XY,โ€11 [8]/47,XY, r(11)(p15.5,q25)x2[2], with minor anomalies and mental retardation who developed asynchronous bilateral Wilms tumors (WTs). Array comparative genomic hybridization (CGH) performed on peripheral bl