MULTIPLE HOLLOW ORGAN DYSPLASIA IN EHLERS-DANLOS SYNDROME

被引:17
作者
SCHIPPERS, E [1 ]
DITTLER, HJ [1 ]
机构
[1] TECH UNIV MUNICH, KLINIKUM RECHTS ISAR, DEPT SURG, D-8000 MUNICH 80, FED REP GER
关键词
D O I
10.1016/S0022-3468(89)80114-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:1181 / 1183
页数:3
相关论文
共 11 条
[1]   HETEROGENEITY OF EHLERS-DANLOS SYNDROME - DESCRIPTION OF 3 CLINICAL TYPES AND A HYPOTHESIS TO EXPLAIN BASIC DEFECT(S) [J].
BARABAS, AP .
BMJ-BRITISH MEDICAL JOURNAL, 1967, 2 (5552) :612-+
[2]   VARIANTS OF EHLERS-DANLOS SYNDROME - CLINICAL BIOCHEMICAL HAEMATOLOGICAL AND CHROMOSOMAL FEATURES OF 100 PATIENTS [J].
BEIGHTON, P ;
PRICE, A ;
LORD, J ;
DICKSON, E .
ANNALS OF THE RHEUMATIC DISEASES, 1969, 28 (03) :228-+
[3]   CLINICAL AND ULTRASTRUCTURAL HETEROGENEITY OF TYPE-IV EHLERS-DANLOS SYNDROME [J].
BYERS, PH ;
HOLBROOK, KA ;
MCGILLIVRAY, B ;
MACLEOD, PM ;
LOWRY, RB .
HUMAN GENETICS, 1979, 47 (02) :141-150
[4]  
Danlos, 1908, B SOC FRANC DERMAT S, V19, P70
[5]  
Ehlers E., 1901, DERMATOLOGISCHE Z, V8, P173
[6]   MORTALITY IN EHLERS-DANLOS SYNDROME DUE TO SPONTANEOUS RUPTURE OF LARGE ARTERIES [J].
MCFARLAND, W ;
FULLER, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1964, 271 (25) :1309-&
[7]  
MCKUSICK VA, 1972, HERITABLE DISORDERS, P293
[8]   EDS-IV (ACROGERIA) - NEW AUTOSOMAL DOMINANT AND RECESSIVE TYPES [J].
POPE, FM ;
JONES, PM ;
WELLS, RS ;
LAWRENCE, D ;
NICHOLLS, AC .
JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 1980, 73 (03) :180-186
[9]   THE EHLERS-DANLOS SYNDROME AND COLONIC PERFORATION - REPORT OF A CASE AND PHYSIOLOGIC ASSESSMENT OF UNDERLYING MOTILITY DISORDER [J].
SIGURDSON, E ;
STERN, HS ;
HOUPT, J ;
ELSHARKAWY, TY ;
HUIZINGA, JD .
DISEASES OF THE COLON & RECTUM, 1985, 28 (12) :962-966