Caudal regression syndrome - case report and review of literature

被引:50
作者
Singh, SK [1 ]
Singh, RD [1 ]
Sharma, A [1 ]
机构
[1] Tulsi Hosp Ltd, Natl Board, Kanpur 208002, Uttar Pradesh, India
关键词
caudal regression syndrome; caudal dysplasia sequence; sacral agenesis; congenital malformations;
D O I
10.1007/s00383-005-1451-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Caudal regression syndrome is a rare disorder of distal spinal segments affecting the development of the spinal cord, with attendant sequelae. Intelligence is preserved. The exact etiology is elusive, though maternal diabetes, genetic factors, and hypoperfusion might play roles. Recently, the role of teratogens has been studied in animal models. Treatment is difficult, multidisciplinary, and largely supportive. Lower limb deformities with sensory and motor loss and neurogenic bladder call for intensive and long-term attention.
引用
收藏
页码:578 / 581
页数:4
相关论文
共 33 条
[1]  
Adra A, 1994, Obstet Gynecol Surv, V49, P508, DOI 10.1097/00006254-199407000-00028
[2]  
Aslan Halil, 2001, BMC Pregnancy Childbirth, V1, P8
[3]  
BENACERRAF BR, 1998, CAUDAL REGRESSION SY, P250
[4]   URODYNAMIC EVALUATION OF CHILDREN WITH THE CAUDAL REGRESSION SYNDROME (CAUDAL DYSPLASIA SEQUENCE) [J].
BOEMERS, TM ;
VANGOOL, JD ;
DEJONG, TPVM ;
BAX, KMA .
JOURNAL OF UROLOGY, 1994, 151 (04) :1038-1040
[5]  
Cama A, 1996, EUR J PEDIATR SURG, V6, P44
[6]   FROM MERMAID TO ANAL IMPERFORATION - SYNDROME OF CAUDAL REGRESSION [J].
DUHAMEL, B .
ARCHIVES OF DISEASE IN CHILDHOOD, 1961, 36 (186) :152-&
[7]   LUMBOSACRAL AGENESIS - 3 CASES OF RECONSTRUCTION USING COTREL-DUBOUSSET OR L-ROD INSTRUMENTATION [J].
DUMONT, CE ;
DAMSIN, JP ;
FORIN, V ;
CARLIOZ, H .
SPINE, 1993, 18 (09) :1229-1235
[8]  
FINER NN, 1978, CLIN GENET, V13, P353
[9]  
Fukada Y, 1999, ACTA OBSTET GYN SCAN, V78, P655
[10]   Sonographic diagnosis of caudal regression in the first trimester of pregnancy [J].
González-Quintero, VH ;
Tolaymat, L ;
Martin, D ;
Romaguera, RL ;
Rodríguez, MM ;
Izquierdo, LA .
JOURNAL OF ULTRASOUND IN MEDICINE, 2002, 21 (10) :1175-1178