LAURENCE-MOON-BIEDL SYNDROME (QUESTIONABLE) AND PRADER-WILLI SYNDROME (QUESTIONABLE) IN A SINGLE FAMILY

被引:10
作者
ENDO, M [1 ]
TASAKA, Y [1 ]
MATSUURA, N [1 ]
MATSUDA, I [1 ]
机构
[1] HOKKAIDO UNIV, SCH MED, DEPT PEDIAT, SAPPORO, HOKKAIDO 060, JAPAN
关键词
D O I
10.1007/BF00444648
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:269 / 276
页数:8
相关论文
共 17 条
[1]  
Alstrom C.H., 1959, ACTA PSYCH NEUROL SC, V129, P1
[2]   PRADER-WILLI SYNDROME IN INFANT MONOZYGOTIC TWINS [J].
BRISSENDEN, JE ;
LEVY, EP .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1973, 126 (01) :110-112
[3]   LAURENCE-MOON-BIEDL SYNDROME - REPORT OF AN UNUSUAL FAMILY [J].
CICCARELLI, E ;
VESELL, ES .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1961, 101 (04) :519-+
[4]   PRADER-WILLI SYNDROME [J].
COHEN, MM ;
GORLIN, RJ .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1969, 117 (02) :213-+
[5]  
DUNN HG, 1968, ACTA PAEDIATR SCAND, VS, P1
[6]   LAURENCE-MOON-BARDET-BIEDL SYNDROME IN ISRAEL [J].
EHRENFELD, EN ;
ROWE, H ;
AUERBACH, E .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1970, 70 (04) :524-+
[7]  
ENDO M, 1975, CLIN ENDOCR JAP, V23, P637
[8]  
GARDNER LI, 1975, ENDOCRINE GENETIC DI, P1324
[9]   ALSTROM SYNDROME - REPORT OF 3 CASES WITH FURTHER DELINEATION OF CLINICAL, PATHOPHYSIOLOGICAL, AND GENETIC ASPECTS OF DISORDER [J].
GOLDSTEIN, JL ;
FIALKOW, PJ .
MEDICINE, 1973, 52 (01) :53-71
[10]   SYNDROME OF LAURENCE-MOON-BARDET-BIEDL AND ALLIED DISEASES IN SWITZERLAND . CLINICAL, GENETIC AND EPIDEMIOLOGICAL STUDIES [J].
KLEIN, D ;
AMMANN, F .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1969, 9 (03) :479-&