GLAUCOMA-LENS ECTOPIA-MICROSPHEROPHAKIA-STIFFNESS-SHORTNESS (GEMSS) SYNDROME - A DOMINANT DISEASE WITH MANIFESTATIONS OF WEILL-MARCHESANI SYNDROMES

被引:25
作者
VERLOES, A
HERMIA, JP
GALAND, A
KOULISCHER, L
DODINVAL, P
机构
[1] STATE UNIV LIEGE,CTR HUMAN GENET,B-4000 LIEGE,BELGIUM
[2] SART TILMAN UNIV HOSP,DEPT OPHTHALMOL,LIEGE,BELGIUM
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 01期
关键词
ECTOPIA LENTIS; GEMSS SYNDROME; MOORE-FEDERMAN SYNDROME; STIFF JOINTS; WEILL-MARCHESANI SYNDROME;
D O I
10.1002/ajmg.1320440112
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a syndrome of progressive joint stiffness, glaucoma, and lens dislocation observed in three generations and compare it with two previous records of short stature, lens ectopia, and articular limitation. This family confirms the existence of a dominant Weill-Marchesani-like syndrome. We suggest that it could be related to the Moore-Federman syndrome. We coin the acronym GEMSS syndrome (Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature) to distinguish this dominant Weill-Marchesani-like syndrome from the classic, recessively inherited syndrome.
引用
收藏
页码:48 / 51
页数:4
相关论文
共 10 条
[1]  
GORLIN RJ, 1974, J PEDIATR OPHTHALMOL, V11, P139
[2]   OCULAR COMPLICATIONS IN WEILL-MARCHESANI SYNDROME [J].
JENSEN, AD ;
CROSS, HE ;
PATON, D .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1974, 77 (02) :261-269
[3]  
KLOEPFER HW, 1955, AM J HUM GENET, V7, P398
[4]   WEILL-MARCHESANI SYNDROME - BRACHYMORPHISM AND ECTOPIA LENTIS [J].
MCGAVIC, JS .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1966, 62 (05) :820-&
[5]  
MCKUSICK VA, 1974, HERITABLE DISORDERS
[6]   FAMILIAL DWARFISM AND STIFF JOINTS - REPORT OF A KINDRED [J].
MOORE, WT ;
FEDERMAN, DD .
ARCHIVES OF INTERNAL MEDICINE, 1965, 115 (04) :398-&
[7]  
PIETRUSCHKA G, 1973, DTSCH GES WESEN, V28, P2011
[8]  
ROUSSEAU H, 1949, B MEM SOC FRANC DOPH, V62, P369
[9]   MOORE-FEDERMAN SYNDROME AND ACROMICRIC DYSPLASIA - ARE THEY THE SAME ENTITY [J].
WINTER, RM ;
PATTON, MA ;
CHALLENER, J ;
MUELLER, RF ;
BARAITSER, M .
JOURNAL OF MEDICAL GENETICS, 1989, 26 (05) :320-325
[10]  
YOUNG ID, 1986, CLIN GENET, V30, P475