Multiple Endocrinal Neoplasia Syndrome
Ahmed Mohiey Ahmed El-Saqqa;
Abstract
Summary and Conclusion
MEN1 and MEN2 are rare autosomal-dominant
hereditary cancer syndromes that express a variety of
endocrine and non-endocrine tumours with the potential for
considerable morbidity and mortality. Clinicians need to be
able to recognize
MEN1 and MEN2 are rare autosomal-dominant
hereditary cancer syndromes that express a variety of
endocrine and non-endocrine tumours with the potential for
considerable morbidity and mortality. Clinicians need to be
able to recognize
Other data
| Title | Multiple Endocrinal Neoplasia Syndrome | Other Titles | متلازمة أورام الغدد الصماء | Authors | Ahmed Mohiey Ahmed El-Saqqa | Keywords | Multiple Endocrinal Neoplasia Syndrome | Issue Date | 2013 | Description | Summary and Conclusion MEN1 and MEN2 are rare autosomal-dominant hereditary cancer syndromes that express a variety of endocrine and non-endocrine tumours with the potential for considerable morbidity and mortality. Clinicians need to be able to recognize |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 116167.pdf | 3.38 MB | Adobe PDF | View/Open |
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