scholarly journals Karyotypic and fluorescent in situ hybridization study of the centromere of chromosome 7 in secondary myeloid neoplasms

2011 ◽  
Vol 33 (6) ◽  
pp. 425-431 ◽  
Author(s):  
Roberta Sandra da Silva Tanizawa ◽  
Cristina Aiko Kumeda ◽  
Raymundo Soares de Azevedo Neto ◽  
Aline de Medeiros Leal ◽  
Patrícia de Barros Ferreira ◽  
...  
2008 ◽  
Vol 39 (4) ◽  
pp. 536-542 ◽  
Author(s):  
Barbara Bernasconi ◽  
Eva Karamitopolou-Diamantiis ◽  
Luigi Tornillo ◽  
Alessandro Lugli ◽  
Dolores Di Vizio ◽  
...  

2008 ◽  
Vol 11 (2) ◽  
pp. 148-151 ◽  
Author(s):  
Diana Negrón ◽  
Lillian Colón-Castillo ◽  
Ilia Morales-Melecio ◽  
María Correa-Rivas

We report a case of a 12-year-old boy with history of myelofibrosis and retinopathy who developed sudden neurological deficits associated with coagulopathy, multiorgan failure, and death. A fluorescent in situ hybridization study revealed monosomy of chromosome 7 in 21% of the bone marrow cells in support of his diagnosis of myelofibrosis. Postmortem neuropathology examination revealed multiple coarse and microcalcifications and cerebral hemorrhages, explaining the patient's neurological deterioration. The findings of myelofibrosis, retinopathy, and cerebral calcifications indicate that this could be a case of a rare condition known as Revesz syndrome.


2013 ◽  
Vol 133 (4) ◽  
pp. 1111-1114 ◽  
Author(s):  
Pierre Sujobert ◽  
Wendy Cuccuini ◽  
Dominique Vignon-Pennamen ◽  
Nadine Martin-Garcia ◽  
Anne Flore Albertini ◽  
...  

2009 ◽  
Vol 456 (1) ◽  
pp. 77-84 ◽  
Author(s):  
Kien T. Mai ◽  
Hamidreza Faraji ◽  
Darren Desantis ◽  
Susan J. Robertson ◽  
Eric C. Belanger ◽  
...  

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