G-SYNDROME - CASE-REPORT

被引：12

作者：

GREENBERG, CR

SCHRAUFNAGEL, D

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1979年 / 3卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320030111

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A case of the G syndrome is reported in a baby boy who had an unusual facies (prominent forehead, telecanthus, posteriorly rotated ears, and anteverted nostrils), laryngeal cleft, hypospadias, cryptorchidism, and psychomotor development delay, possibly secondary to birth asphyxia and numerous medical and surgical complications. The mother had a similar facies.

引用

页码：59 / 64

页数：6

共 12 条

[1] G-SYNDROME [J].

COBURN, TP .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1970, 120 (05) :466-&

[2]

CORDERO JF, 1977, PEDIATR RES, V11, P524, DOI 10.1203/00006450-197704000-00929

[3]

FRIAS JL, 1972, BIRTH DEFECTS OAS, V11, P54

[4]

GILBERT EF, 1972, Z KINDERHEILKD, V11, P290

[5]

GORLIN RJ, 1976, SYNDROMES HEAD NECK, P386

[6]

KASNER J, 1974, Z KINDERHEILKD, V118, P81

[7] G-SYNDROME [J].

LITTLE, JR ;

OPITZ, JM .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1971, 121 (06) :505-&

[8] HYPERTELORISM-HYPOSPADIAS SYNDROME WITH A LARYNGOTRACHEOESOPHAGEAL CLEFT [J].

MILLER, PR ;

BERNSTEIN, RM ;

PATHAK, A ;

DECANCQ, HG .

JOURNAL OF PEDIATRICS, 1977, 90 (01) :157-158

[9]

OPITZ J M, 1969, Birth Defects Original Article Series, V5, P95

[10] G SYNDROME - 4-GENERATION FAMILY STUDY [J].

PEDERSEN, IL ;

MIKKELSEN, M ;

OSTER, J .

HUMAN HEREDITY, 1976, 26 (01) :66-71

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