Caudal Regression Syndrome: Clinical Case and Update

被引:0
作者
Luque H, Maria Jose [1 ]
Fernandez B, Rocio [1 ]
Tuca D, Maria Jesus [1 ]
Luco, Matias, I [3 ]
De Barbieri M, Florencia [2 ]
Tapia, Jose Luis, I [3 ]
机构
[1] Pontificia Univ Catolica Chile, Escuela Med, Fac Med, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Dept Radiol, Unidad Radiol Pediat, Fac Med, Santiago, Chile
[3] Pontificia Univ Catolica Chile, Dept Pediat, Unidad Neonatol, Fac Med, Santiago, Chile
来源
REVISTA CHILENA DE PEDIATRIA-CHILE | 2010年 / 81卷 / 02期
关键词
Caudal regression syndrome; caudal dysplasia; sacral agenesis; diabetes; spinal dysraphia;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Caudal regression is a rare congenital malformation which includes a wide spectrum of musculoskeletal abnormalities involving the lumbosacral spine, pelvis and lover limbs. It can be associated to visceral defects (gastrointestinal, genitourinary, cardiac or neurological) in various degrees. The etiology is not yet clear, but maternal diabetes, genetic predisposition, and vascular hypoperfusion are suspected. Objective: Describe a case of exceptional extension, including first year evolution. Clinical Case: A male newborn, term, was diagnosed before birth. Mother is a Type 2 diabetic. Physical exam and images confirm the diagnosis, show presence of 7 cervical vertebrae, 8 thoracic, agenesia of distal dorsal and lumbosacral spine. No spinal disraphia, medular conus at D2. Conclusion: The reported case shows that early diagnosis and multidisciplinary evaluation of the patient arc essential elements to decrease complications and improve prognosis.
引用
收藏
页码:148 / 154
页数:7
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