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Other purported endocrine tumor syndromes have been suggested either as new entities or as subtypes of the existing MEN syndromes. The evidence in favor of these contentions is examined critically. Only one \u201cnew\u201d association. That of pheochro\u2010mocytomas and islet cell tumors, seems reasonable, and even in this setting, some relatives have had manifestations of von Hippel\u2010Lindau syndrome. There is no compelling reason why such conditions as von Hippel\u2010Lindau syndrome, peripheral neuro\u2010fibromatosis, McCune\u2010Albright syndrome, and others should be reclassified as MEN syndromes, although awareness of their collective endocrine abnormalities is clinically important.<\/jats:p>","DOI":"10.1002\/ajmg.1320370317","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:52:22Z","timestamp":1118548342000},"page":"375-383","source":"Crossref","is-referenced-by-count":38,"title":["Multiple endocrine neoplasia: How many syndromes?"],"prefix":"10.1002","volume":"37","author":[{"given":"R. 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