PALLISTER-HALL SYNDROME AND MCKUSICK-KAUFMANN SYNDROME - ONE ENTITY

被引:33
作者
UNSINN, KM
NEU, N
KREJCI, A
POSCH, A
MENARDI, G
GASSNER, I
机构
[1] UNIV INNSBRUCK, CHILDRENS HOSP, A-6020 INNSBRUCK, AUSTRIA
[2] UNIV INNSBRUCK HOSP, DEPT MRI, A-6020 INNSBRUCK, AUSTRIA
[3] UNIV INNSBRUCK HOSP, DEPT PAEDIAT SURG, A-6020 INNSBRUCK, AUSTRIA
关键词
D O I
10.1136/jmg.32.2.125
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Pallister-Hall syndrome is characterised by specific facial anomalies, postaxial polydactyly, imperforate anus, and brain anomalies including a diencephalic hamartoblastoma. The hallmarks of the McKusick-Kaufmann syndrome are hydrocolpos owing to vaginal atresia, postaxial polydactyly, imperforate anus, and congenital heart defects. We report a patient with the unique features of hydrocolpos, postaxial polydactyly, and hypothalamic hamartoblastoma and discuss the different aetiological considerations of both syndromes and implications for clinical management.
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收藏
页码:125 / 128
页数:4
相关论文
共 14 条
[11]  
MCKUSICK KA, 1964, JAMA-J AM MED ASSOC, V89, P813
[12]  
REED MH, 1973, AM J ROENTGENOL, V118, P1
[13]   RECURRENCE OF PALLISTER-HALL SYNDROME IN 2 SIBS [J].
THOMAS, HM ;
TODD, PJ ;
HEAF, D ;
FRYER, AE .
JOURNAL OF MEDICAL GENETICS, 1994, 31 (02) :145-147
[14]   AUTOSOMAL-DOMINANT TRANSMISSION OF THE PALLISTER-HALL SYNDROME [J].
TOPF, KF ;
KLETTER, GB ;
KELCH, RP ;
BRUNBERG, JA ;
BIESECKER, LG .
JOURNAL OF PEDIATRICS, 1993, 123 (06) :943-946