C-TRIGONOCEPHALY SYNDROME - CLINICAL VARIABILITY AND POSSIBILITY OF SURGICAL-TREATMENT

被引:18
作者
LALATTA, F
BAGOZZI, DC
SALMOIRAGHI, MG
TAGLIABUE, P
TISCHER, C
ZOLLINO, M
DIROCCO, C
NERI, G
OPITZ, JM
机构
[1] OSPED NUOVO S GERARDO, MONZA, ITALY
[2] SHODAIR CHILDRENS HOSP, HELENA, MT USA
[3] UNIV CATTOLICA SACRO CUORE, FAC MED A GEMELLI, IST NEUROCHIRURG, I-00168 ROME, ITALY
[4] UNIV CATTOLICA SACRO CUORE, FAC MED A GEMELLI, IST GENET UMANA, I-00168 ROME, ITALY
[5] UNIV MILAN, CATTEDRA PATOL NEONATALE, I-20122 MILAN, ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 37卷 / 04期
关键词
craniosynostectomy; craniosynostosis; mental retardation; omphalocele; recessive inheritance;
D O I
10.1002/ajmg.1320370404
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on 3 new cases of C trigonocephaly syndrome. In addition to the findings characteristic of this condition, one of the patients also had a large omphalocele. This patient was referred from a suburban hospital with a diagnosis of Down syndrome, stressing the fact that C syndrome is still under-recognized and underdiagnosed. Another patient was diagnosed at birth and immediately submitted to craniosynostectomy. A second operation was performed 7 months later resulting in normal brain growth and close to normal psychomotor development at 3 years, in contrast to the third patient, who was not treated surgically and was severely retarded at 4 years.
引用
收藏
页码:451 / 456
页数:6
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