Article
Concepts for screening and diagnostic follow-up in multiple endocrine neoplasia type 1 (MEN1).
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association - 1 Jan 2000
Karges W, Schaaf L, Dralle H, Boehm B O
Abstract excerpt
The recent identification of MEN1 gene mutations as the molecular cause of familial multiple endocrine neoplasia type 1 syndrome (MEN1) has had a significant impact on clinical patient care. In the following consensus statement we will present recommendations for clinical screening and follow-up in patients and relatives with suspected or established MEN1 syndrome. MEN1 mutational analysis should be performed in...
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