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10.1159/000441528 http://scihub22266oqcxt.onion/10.1159/000441528 C4881270!4881270!27239450     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Ocul+Oncol+Pathol 2016 ; 2 (3): 128-32 Nephropedia Template TP {{tp|p=27239450|t=2016. Clinical Presentation and Genetic Paradigm of Diffuse Infiltrating Retinoblastoma: A Review |pdf=|usr=}}{{27239450}} gab.com Text Clinical Presentation and Genetic Paradigm of Diffuse Infiltrating Retinoblastoma: A Review JO: Ocul Oncol Pathol http://www.kidney.de/pget.php?&tw=1&pmid=27239450 #FOAvip Retinoblastoma is the most common childhood cancer. Thanks to modern technology and good medical access, mortality in Europe has decreased to about 5%. Diffuse infiltrating retinoblastoma is a very rare subtype of this neoplasm and is characterized by its atypical growth pattern. Diffuse infiltrating retinoblastoma may mimic other more innocuous diseases and may therefore be misdiagnosed. The purpose of this paper was to provide a short review of the main symptoms of diffuse infiltrating retinoblastoma presenting to the ophthalmologist and give a comparison to typical retinoblastoma. The second purpose was to set up a discussion of the genetic paradigm of diffuse infiltrating retinoblastoma. It has often been described to occur sporadically; however, in the last years, it has been shown that it might be heritable. A literature search concerning diffuse infiltrating retinoblastoma considering English, German and Spanish cases and case series identified 77 patients. Moreover, an overview of general data, main symptoms, clinical findings and initial working diagnoses or referral diagnoses is given. Males were significantly more often affected than females. Diffuse infiltrating retinoblastoma can be heritable. Genetic analysis should be offered to the patient and relatives. Interdisciplinary medical follow-up care is needed to detect associated cancers. Twit Text FOAVip Clinical Presentation and Genetic Paradigm of Diffuse Infiltrating Retinoblastoma: A Review ????Ocul Oncol Pathol http://www.kidney.de/pget.php?&tw=1&pmid=27239450 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27239450 #FOAvip English Wikipedia <ref>{{Cite pmid|27239450}}</ref> Clinical Presentation and Genetic Paradigm of Diffuse Infiltrating Retinoblastoma: A Review #MMPMID27239450 Traine PG; Schedler KJ; Rodrigues EB Ocul Oncol Pathol 2016[Apr]; 2 (3): 128-32 PMID27239450show ga Retinoblastoma is the most common childhood cancer. Thanks to modern technology and good medical access, mortality in Europe has decreased to about 5%. Diffuse infiltrating retinoblastoma is a very rare subtype of this neoplasm and is characterized by its atypical growth pattern. Diffuse infiltrating retinoblastoma may mimic other more innocuous diseases and may therefore be misdiagnosed. The purpose of this paper was to provide a short review of the main symptoms of diffuse infiltrating retinoblastoma presenting to the ophthalmologist and give a comparison to typical retinoblastoma. The second purpose was to set up a discussion of the genetic paradigm of diffuse infiltrating retinoblastoma. It has often been described to occur sporadically; however, in the last years, it has been shown that it might be heritable. A literature search concerning diffuse infiltrating retinoblastoma considering English, German and Spanish cases and case series identified 77 patients. Moreover, an overview of general data, main symptoms, clinical findings and initial working diagnoses or referral diagnoses is given. Males were significantly more often affected than females. Diffuse infiltrating retinoblastoma can be heritable. Genetic analysis should be offered to the patient and relatives. Interdisciplinary medical follow-up care is needed to detect associated cancers. äClinical Presentation and Genetic Paradigm of Diffuse Infiltrating Ret(epmc).pdf DeepDyve Pubget Overpricing