Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas

@inproceedings{Miric2016RecentAI,
  title={Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas},
  author={Alexandra Mirică and Ioana Anca Bădărău and Radu Mihail Mirica and Sorin Păun and Cătălina Poiană and Diana Loreta Păun},
  year={2016}
}
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors, which secrete catecholamines, with the same embryological origin from the neural crest cells. Pheochromocytomas develop from the adrenal medulla, while paragangliomas are extraadrenal tumors, evolving from the autonomic sympathetic and parasympathetic nervous chains. In the last 10 years, molecular medicine has discovered novelties in the understanding of genetics of these tumors. Although the majority of these tumors occur… CONTINUE READING

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Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Adrenal MedullaIs normal tissue origin of diseasePheochromocytoma
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas .
In this article we have reviewed the current medical literature , in order to summarise the most important aspects of genetics and clinical features of pheochromocytomas and paragangliomas .
In addition to this , developments in molecular pathology of pheochromocytomas and paragangliomas will provide the key to target specifi c cellular markers , assuring a personalised therapy .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas .
In this article we have reviewed the current medical literature , in order to summarise the most important aspects of genetics and clinical features of pheochromocytomas and paragangliomas .
In addition to this , developments in molecular pathology of pheochromocytomas and paragangliomas will provide the key to target specifi c cellular markers , assuring a personalised therapy .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
In addition to this , developments in molecular pathology of pheochromocytomas and paragangliomas will provide the key to target specifi c cellular markers , assuring a personalised therapy .
In this article we have reviewed the current medical literature , in order to summarise the most important aspects of genetics and clinical features of pheochromocytomas and paragangliomas .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
In addition to this , developments in molecular pathology of pheochromocytomas and paragangliomas will provide the key to target specifi c cellular markers , assuring a personalised therapy .
In this article we have reviewed the current medical literature , in order to summarise the most important aspects of genetics and clinical features of pheochromocytomas and paragangliomas .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
Recent Advances in the Genetics of Pheochromocytomas and Paragangliomas .
Pheochromocytomas develop from the adrenal medulla , while paragangliomas are extraadrenal tumors , evolving from the autonomic sympathetic and parasympathetic nervous chains .
In addition to this , developments in molecular pathology of pheochromocytomas and paragangliomas will provide the key to target specifi c cellular markers , assuring a personalised therapy .
In this article we have reviewed the current medical literature , in order to summarise the most important aspects of genetics and clinical features of pheochromocytomas and paragangliomas .
Paragangliomas and pheochromocytomas are rare neuroendocrine tumors , which secrete catecholamines , with the same embryological origin from the neural crest cells .
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