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MON-LB059 A Family Reunion at the Geneticist's Office: Hypercalcemia as Presenting Symptoms of MEN1
Background: MEN1 syndrome is an autosomal dominant disorder of the MEN1 gene, which encodes the tumor suppressor protein menin, characterized by primary hyperparathyroidism, pituitary and gastro-entero-pancreatic tract tumors. Patients typically present in the second decade of life with primary hype...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550704/ http://dx.doi.org/10.1210/js.2019-MON-LB059 |