POSSIBLE RELATIONSHIP BETWEEN ULNAR-MAMMARY SYNDROME AND SPLIT HAND WITH APLASIA OF THE ULNA SYNDROME

被引:15
|
作者
FRANCESCHINI, P [1 ]
VARDEU, MP [1 ]
DALFORNO, L [1 ]
SIGNORILE, F [1 ]
FRANCESCHINI, D [1 ]
LALA, R [1 ]
MATARAZZO, P [1 ]
机构
[1] OSPED INFANTILE R MARGHERITA,DIV ENDOCRINOL PEDIAT,TURIN,ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 06期
关键词
SCHINZEL SYNDROME; ULNARMAMMARY SYNDROME; SPLIT HAND WITH APLASIA OF THE ULNA SYNDROME; ULNAR RAY DEFECTS; SPLIT-HAND; STIFF INTERPHALANGEAL JOINTS; DENTAL ANOMALIES; APOCRINE GLAND HYPOPLASIA; MAMMARY GLAND HYPOPLASIA; ABSENT AXILLARY HAIR; DELAYED PUBERTY; HYPOGENITALISM; OBESITY;
D O I
10.1002/ajmg.1320440618
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe a 3-generation family in which mother, maternal grandfather, and 2 (male and female) children have variably manifestations of the ulnar-mammary syndrome, including ulnar ray defects, obesity, hypogenitalism, delayed puberty, hypoplasia of nipples and apocrine glands, and a previously undescribed ectopia of upper canines. The index patient also had split-hand appearance on the right due to complete absence of the 4th ray. To our knowledge this is the first documented example of split hand in the ulnar-mammary syndrome. The hand anomaly raises the question of a possible causal relationship between ulnar-mammary syndrome and the split hand with aplasia of the ulna syndrome, as already hypothesized by Lenz [1980].
引用
收藏
页码:807 / 812
页数:6
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