Prenatal diagnosed caudal regression syndrome
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چکیده
منابع مشابه
Prenatal diagnosed caudal regression syndrome
Background: Caudal regression syndrome (CRS) is a rare complex congenital anomaly which is characterized by agenesis of the sacral and lumbar spine. Pelvis, lower extremity, genitourinary, cardiac anomalies and lower extremity neurological and motor development deficits may be accompanied. The exact etiology is unclear but the maternal insulin-dependent diabetes mellitus (hyperglycaemia during ...
متن کاملPrenatal diagnosis of caudal regression syndrome without maternal diabetes mellitus.
Caudal regression syndrome is a rare congenital malformation with varying degrees of early gestational developmental failure. It is also known as sacral agenesis or caudal dysplasia. The cause of this malformation is thought to be defects in neuralization around the 28th day of the gestational period. Although maternal uncontrolled diabetes, genetic predisposition and vascular hypoperfusion are...
متن کاملPrenatal diagnosis of Caudal Regression Syndrome : a case report
BACKGROUND: Caudal regression is a rare syndrome which has a spectrum of congenital malformations ranging from simple anal atresia to absence of sacral, lumbar and possibly lower thoracic vertebrae, to the most severe form which is known as sirenomelia. Maternal diabetes, genetic predisposition and vascular hypoperfusion have been suggested as possible causative factors. CASE PRESENTATION: We r...
متن کاملCaudal Regression Syndrome
Caudal regression syndrome (CRS) is a rare neural tube defect affecting terminal spinal segments and cord manifesting as neurological deficit ranging from bladder and bowel involvement to severe sensory motor deficits in lower limbs. It has sporadic appearance and maternal diabetes, genetic factors, teratogens and hypoperfusion are considered as possible etiologic factors and it can be associat...
متن کاملCaudal regression syndrome.
INTRODUCTION The regression caudal syndrome includes a spectrum of malformations which vary from the symptomless coccygeal agenesis until thoracic vertebrae and sacrococcygeal agenesis with severe neurological deficit; it is associated sometimes with malformations in other organs and systems. We present a case of partial agenesis of sacro and coccix with neuromuscular, sphincter and orthopedist...
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ژورنال
عنوان ژورنال: Open Journal of Obstetrics and Gynecology
سال: 2013
ISSN: 2160-8792,2160-8806
DOI: 10.4236/ojog.2013.32042