A NEW SKELETAL DYSPLASIA IN 2 UNRELATED BOYS

被引:19
作者
SAUL, RA
WILSON, WG
机构
[1] UNIV VIRGINIA,MED CTR,HLTH SCI CTR,DEPT PEDIAT,BOX 386,CHARLOTTESVILLE,VA 22908
[2] GREENWOOD GENET CTR,GREENWOOD,SC 29646
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 35卷 / 03期
关键词
Malformation syndrome floating-harbor syndrome; Short stature; Sporadic occurrence;
D O I
10.1002/ajmg.1320350315
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on 2 unrelated boys with similar physical and radiographic findings that may represent a 'new' skeletal dysplasia. Findings in common include early speech delay, short stature, frontal bossing with a depression over the metopic suture, a narrow nasal root with beaked nose, midfacial hypoplasia with relatively prominent eyes, and brachydactyly with blunt fingers. Radiographic findings include mild irregularities of the vertebral bodies, hypoplasia of the odontoid process, short phalanges with increased distal width, coning and sclerosis of several epiphyses, and overtubulation of the long bones. Although these patients share some manifestations with the floating-harbor syndrome (Robinson et al.: J Pediatr 113:703-706, 1988), their radiographic changes are distinctive and are not suggestive of a recognized skeletal dysplasia syndrome.
引用
收藏
页码:388 / 393
页数:6
相关论文
共 3 条
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LEISTI J, 1974, SYNDROME IDENTIFICAT, V2, P3
[2]  
Pelletier G., 1973, SYNDROME IDENTIFICAT, V1, P8
[3]   A UNIQUE ASSOCIATION OF SHORT STATURE, DYSMORPHIC FEATURES, AND SPEECH IMPAIRMENT (FLOATING-HARBOR SYNDROME) [J].
ROBINSON, PL ;
SHOHAT, M ;
WINTER, RM ;
CONTE, WJ ;
GORDONNESBITT, D ;
FEINGOLD, M ;
LARON, Z ;
RIMOIN, DL .
JOURNAL OF PEDIATRICS, 1988, 113 (04) :703-706