2008
DOI: 10.1007/s00590-008-0347-0
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Orthopaedic management of caudal regression syndrome

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Cited by 7 publications
(7 citation statements)
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“…Caudal regression is a complicated syndrome of dysgenesis characterized by abnormal formation of the distal spine and pelvis [1,2,3,4]. Our case demonstrated an array of orthopedic, neurologic, and urologic abnormalities.…”
Section: Discussionmentioning
confidence: 88%
“…Caudal regression is a complicated syndrome of dysgenesis characterized by abnormal formation of the distal spine and pelvis [1,2,3,4]. Our case demonstrated an array of orthopedic, neurologic, and urologic abnormalities.…”
Section: Discussionmentioning
confidence: 88%
“…Caudal regression syndrome is rare congenital malformation associated with severe skeletal deficiencies of the vertebral or sacrococcygeal bones, resulting in complex anomalies in the gastrointestinal, neural, orthopedic, and genitourinary system [2 , 4] . This syndrome is characterized by complex dysraphism with aberrations in gastrulation and failure of notochord formation.…”
Section: Discussionmentioning
confidence: 99%
“…The patients with unstable spino-pelvic structure must be observed for the progressing spinal deformity and instability (indicated by worsening of the body posture) with the associated trunk shortening and abdominal collapse which further cause multiple organ problems ranging from the cardiorespiratory, gastrointestinal, and the urogenital. Thus, the management of Pang type I CRS is more likely to provide support and to improve the residual function than to correct deformities [4] . Spinal brace, sub-throchanteric amputations with pelvic thoracic prosthesis, or spino-pelvic fusion without or with multilevel pedicular screw fixation were options reported in various literatures [3 , 5 , 12 , 15 , 16] .…”
Section: Discussionmentioning
confidence: 99%
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