HYPERPHALANGISM, FACIAL ANOMALIES, HALLUX-VALGUS, AND BRONCHOMALACIA - A NEW SYNDROME

被引：12

作者：

CHITAYAT, D

HAJCHAHINE, S

STALKER, HJ

AZOUZ, EM

COTE, A

HALAL, F

机构：

[1] MONTREAL CHILDRENS HOSP,DEPT PEDIAT,DIV MED GENET,MONTREAL H3H 1P3,QUEBEC,CANADA

[2] MONTREAL CHILDRENS HOSP,CTR HUMAN GENET,MONTREAL H3H 1P3,QUEBEC,CANADA

[3] MONTREAL CHILDRENS HOSP,DIV PATHOL,MONTREAL H3H 1P3,QUEBEC,CANADA

[4] MONTREAL CHILDRENS HOSP,DIV RADIOL,MONTREAL H3H 1P3,QUEBEC,CANADA

[5] MONTREAL CHILDRENS HOSP,DIV RESP MED,MONTREAL H3H 1P3,QUEBEC,CANADA

[6] MCGILL UNIV,MONTREAL H3A 2T5,QUEBEC,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 45卷 / 01期

关键词：

HYPERPHALANGISM; ACCESSORY PHALANGES; HYPOSPADIAS; RESPIRATORY DISTRESS; HALLUX VALGUS; BRONCHOMALACIA;

D O I：

10.1002/ajmg.1320450103

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We report on a boy with hyperphalangism, partial syndactyly, facial anomalies, and diffuse bronchomalacia, born to a nonconsanguineous French-Canadian couple. To our knowledge, this is a hitherto undescribed syndrome.

引用

页码：1 / 4

页数：4

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