The genetics of male undermasculinization

被引:47
作者
Ahmed, SF
Hughes, IA
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Paediat, Cambridge CB2 2QQ, England
[2] Univ Glasgow, Royal Hosp Sick Children, Dept Child Hlth, Glasgow, Lanark, Scotland
关键词
D O I
10.1046/j.1365-2265.2002.01430.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A review of the genetics of male undermasculinization must encompass a description of the embryology of the genital system. The dimorphism of sex development consequent upon the formation of a testis and the subsequent secretion of hormones to impose a male phenotype is highlighted. Thus, an understanding of the causes of male undermasculinization (manifest as XY sex reversal, complete and partial) includes reviewing the genetic factors which control testis determination and the production and action of testicular hormones. The study of disorders of male sex development has contributed substantially to knowledge of normal male development before birth. This knowledge has been complimented in recent years by the use of targeted murine gene disruption experiments to study the sex phenotype, although murine and human phenotypes are not always concordant. The investigation of disorders associated with male undermasculinization of prenatal onset is described briefly to complete the review.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 172 条
[41]   IMMUNOHISTOCHEMICAL EVIDENCE FOR DIFFERENTIAL DISTRIBUTION OF 5-ALPHA-REDUCTASE ISOENZYMES IN HUMAN SKIN [J].
EICHELER, W ;
DREHER, M ;
HOFFMANN, R ;
HAPPLE, R ;
AUMULLER, G .
BRITISH JOURNAL OF DERMATOLOGY, 1995, 133 (03) :371-376
[42]   A number of schizencephaly patients including 2 brothers are heterozygous for germline mutations in the homeobox gene EMX2 [J].
Faiella, A ;
Brunelli, S ;
Granata, T ;
DIncerti, L ;
Cardini, R ;
Lenti, C ;
Battaglia, G ;
Boncinelli, E .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1997, 5 (04) :186-190
[43]   LOCALIZATION OF THE HUMAN CYP17 GENE (CYTOCHROME-P45017-ALPHA) TO 10Q24.3 BY FLUORESCENCE INSITU HYBRIDIZATION AND SIMULTANEOUS CHROMOSOME-BANDING [J].
FAN, YS ;
SASI, R ;
LEE, C ;
WINTER, JSD ;
WATERMAN, MR ;
LIN, CC .
GENOMICS, 1992, 14 (04) :1110-1111
[44]   CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].
FOSTER, JW ;
DOMINGUEZSTEGLICH, MA ;
GUIOLI, S ;
KWOK, C ;
WELLER, PA ;
STEVANOVIC, M ;
WEISSENBACH, J ;
MANSOUR, S ;
YOUNG, ID ;
GOODFELLOW, PN ;
BROOK, JD ;
SCHAFER, AJ .
NATURE, 1994, 372 (6506) :525-530
[45]   ANIRIDIA-WILMS TUMOR ASSOCIATION - EVIDENCE FOR SPECIFIC DELETION OF 11P13 [J].
FRANCKE, U ;
HOLMES, LB ;
ATKINS, L ;
RICCARDI, VM .
CYTOGENETICS AND CELL GENETICS, 1979, 24 (03) :185-192
[46]  
Fukami M., 1995, CLIN PEDIAT ENDOCRIN, V4, P39, DOI [10.1297/cpe.4.39, DOI 10.1297/CPE.4.39]
[47]   MALE PSEUDOHERMAPHRODITISM CAUSED BY MUTATIONS OF TESTICULAR 17-BETA-HYDROXYSTEROID DEHYDROGENASE-3 [J].
GEISSLER, WM ;
DAVIS, DL ;
WU, L ;
BRADSHAW, KD ;
PATEL, S ;
MENDONCA, BB ;
ELLISTON, KO ;
WILSON, JD ;
RUSSELL, DW ;
ANDERSSON, S .
NATURE GENETICS, 1994, 7 (01) :34-39
[48]   The alpha-thalassemia mental retardation syndromes [J].
Gibbons, RJ ;
Higgs, DR .
MEDICINE, 1996, 75 (02) :45-52
[49]  
Giuili G, 1997, DEVELOPMENT, V124, P1799
[50]  
Graves JAM, 1998, BIOESSAYS, V20, P264, DOI 10.1002/(SICI)1521-1878(199803)20:3&lt