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SUN-283 FH Variant in a Child with Family History of Early-Onset Pheochromocytoma
Pheochromocytoma (PCC) and paraganglioma (PGL) are rare neuroendocrine tumors associated with many genes. Recently, the fumarate hydratase gene (FH) has been implicated. We describe a case of a child evaluated for PCC who was found to have a variant in FH. A 7y5mo female was referred to our pediatri...
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| Publicado no: | J Endocr Soc |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6552710/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-283 |
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