Journal article
Multiple endocrine neoplasia type 1 (MEN1) in two Asian families
BT Teh, SI Hii, R David, V Parameswaran, S Grimmond, MK Walters, TT Tan, DJ Nancarrow, SP Chan, J Mennon, C Larsson, A Zaini, BAK Khalid, JJ Shepherd, DP Cameron, NK Hayward
Human Genetics | SPRINGER VERLAG | Published : 1994
DOI: 10.1007/BF00211009
Abstract
Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disease characterized by neoplasia of the parathyroid glands, anterior pituitary and endocrine pancreas, is rarely reported in Asian populations. The MEN1 gene, mapped to chromosome 11q13 but yet to be cloned, has been found to be homogeneous in Caucasian populations through linkage analysis. Here, two previously unreported Asian kindreds with MEN1 are described; link-age analysis using microsatellite polymorphic markers in the MEN1 region was carried out. The first kindred, of Mongolian-Chinese origin, is a multigeneration family with over 150 living members, eight of whom are affected to © 1994 Springer-Verlag.