Hyperlordosis

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Prenatal diagnosis of benign extreme hyperlordosis.

etal malposition due to persistent hyperextension of the lumbar spine (hyperlordosis) has only very rarely been reported.1 A literature research (key words: hyperlordosis, hyperextension, lumbar spine, opisthotonus, and prenatal) revealed only 1 published case with prenatal diagnosis.2 We describe a case detected by routine prenatal screening, review the literature, and discuss possible etiolog...

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Case Report: A New Surgical Approach to Cervical Hyperlordosis

INTRODUCTION Cervical hyperlordosis is a rare pediatric deformity leading to gaze and postural disturbances. The cornerstone of treatment consists of spinal manipulative therapy (SMT) combined with positional traction. CASE PRESENTATION We report a new surgical approach in a 7-year-old female patient suffering from stiff cervical hyperlordosis, desiring to correct forward head posture as well...

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Hyperlordosis as a possible factor in the development of spinal cord infarction.

A patient developed persistent symptoms and signs suggestive of partial spinal cord infarction after an operation involving the use of the hyperlordotic position. This position involves extension at the waist, such that both the head and feet are below the level of the waist. It is employed to increase surgical access to the abdomen. Where this position is adopted for a prolonged surgical proce...

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Hyperlordosis is Associated With Facet Joint Pathology at the Lower Lumbar Spine.

STUDY DESIGN A retrospective study. OBJECTIVE Our study opted to clarify the remaining issues of lumbar lordosis (LL) with regard to (1) its physiological values, (2) age, (3) sex, and (4) facet joint (FJ) arthritis and orientation using computed tomography (CT) scans. SUMMARY OF BACKGROUND DATA Recent studies have questioned whether LL really decreases with age, but study sample sizes have...

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Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report

BACKGROUND Hyperlordosis is common in facioscapulohumeral muscular dystrophy (FSHD), which cannot be controlled by bracing. While the surgical treatment is neither reported nor recommended in previous studies, we report the first corrective surgery for hyperlordosis in one wheelchair-dependent FSHD patient. CASE PRESENTATION A 15-year-old, wheelchair-dependent girl complaining of hyperlordosi...

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ژورنال

عنوان ژورنال: British Journal of Anaesthesia

سال: 2003

ISSN: 0007-0912

DOI: 10.1093/bja/aeg626