NEW MANIFESTATIONS OF NEU-LAXOVA SYNDROME

被引：24

作者：

NAVEED, MCS

SREENIVAS, V

机构：

[1] GOVT MED COLL,DEPT PEDIAT,MYSORE,INDIA

[2] GOVT MED COLL,DEPT PATHOL,MYSORE,INDIA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 35卷 / 01期

关键词：

Generalized hydrops; Ichthyosis; Multiple congenital abnormalities; Neural tube defects;

D O I：

10.1002/ajmg.1320350110

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

We report on a newborn boy with Neu-Laxova syndrome and spina bifida, bilateral cryptorchidism, and shallow orbital cavities. Association of these manifestations in Neu-Laxova syndrome is the first to be reported in the literature. This is the first report of Neu-Laxova syndrome from India.

引用

页码：55 / 59

页数：5

共 11 条

[1]

THE NEU-LAXOVA SYNDROME - COMMENTS ON SYNDROME IDENTIFICATION [J].

FITCH, N ;

RESCH, L ;

ROCHON, L .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (04) :445-452

[2]

NEU-LAXOVA SYNDROME - REPORT OF A CASE AND COMMENTS [J].

KARIMINEJAD, MH ;

KHAJAVI, H ;

GHARAVI, MJ ;

KARIMINEJAD, R .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (01) :17-23

[3]

LAXOVA R, 1972, J MENT DEFIC RES, V16, P139

[4]

NEU-LAXOVA SYNDROME - DISTINCT ENTITY [J].

LAZJUK, GI ;

LURIE, IW ;

OSTROWSKAJA, TI ;

CHERSTVOY, ED ;

KIRILLOVA, IA ;

NEDZVED, MK ;

USOEV, SS .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03) :261-267

[5]

NEU-LAXOVA SYNDROME - 2 FURTHER CASE-REPORTS AND COMMENTS ON PROPOSED SUBCLASSIFICATION [J].

MUELLER, RF ;

WINTER, RM ;

NAYLOR, CPE ;

OPITZ, JM .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (04) :645-649

[6]

NEU RL, 1971, PEDIATRICS, V47, P610

[7]

PAES B, 1985, J CLIN DYSMORPHOL, V31, P21

[8]

POVYSILOVA V, 1979, CESK PEDIATR, V31, P190

[9]

NEU-LAXOVA SYNDROME AND CAD COMPLEX - COMMENTS [J].

SCOTT, CI ;

LOURO, JM ;

LAURENCE, KM ;

TOLAROVA, M ;

HALL, JG ;

REED, S ;

CURRY, CJR .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02) :165-175

[10]

ADDITIONAL MANIFESTATIONS OF THE NEU-LAXOVA SYNDROME [J].

TURKEL, SB ;

EBBIN, AJ ;

TOWNER, JW .

JOURNAL OF MEDICAL GENETICS, 1983, 20 (03) :227-229

← 1 2 →