NASOPHARYNGEAL TERATOMA (HAIRY POLYP), DANDY-WALKER MALFORMATION, DIAPHRAGMATIC-HERNIA, AND OTHER ANOMALIES IN A FEMALE INFANT

被引：21

作者：

AUGHTON, DJ

SLOAN, CT

MILAD, MP

HUANG, TE

MICHAEL, C

HARPER, C

机构：

[1] WILLIAM BEAUMONT HOSP,DEPT OBSTET & GYNECOL,ROYAL OAK,MI 48072

[2] WILLIAM BEAUMONT HOSP,DEPT ANAT PATHOL,ROYAL OAK,MI 48072

[3] WILLIAM BEAUMONT HOSP,REPROD GENET PROGRAM,ROYAL OAK,MI 48072

来源：

JOURNAL OF MEDICAL GENETICS | 1990年 / 27卷 / 12期

关键词：

D O I：

10.1136/jmg.27.12.788

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Nasopharyngeal teratomas are rare and are infrequently associated with extra-oral malformations. The case of premature female infant with multiple congenital anomalies, including nasopharyngeal teratoma, Dandy-Walker malformation, diaphragmatic hernia, and congenital heart defect, is presented. This constellation of malformations does not appear to have been reported previously.

引用

页码：788 / 790

页数：3

共 10 条

[1] HYDROLETHALUS SYNDROME - REPORT OF AN APPARENT MILD CASE, LITERATURE-REVIEW, AND DIFFERENTIAL-DIAGNOSIS [J].