The normal structure of the spinal vertebrae is important for maintaining posture and the normal function of the thoracoabdominal organs and nervous system. Kyphoscoliosis occurs when the spinal vertebrae curve excessively beyond their physiological curvature to the back and side. Congenital kyphoscoliosis, a type of kyphoscoliosis, develops in the fetal period and is present in early childhood. However, neither the mechanism of pathogenesis nor the responsible gene has been identified. The lack of established animal models is a significant hurdle that limits the study of congenital kyphoscoliosis. Over the past 15 years, we have been accumulating data on this issue using rat models, based on the idea that the development of congenital kyphoscoliosis is caused by the abnormal expression of genes involved in normal bone formation. We hypothesize that analysis of an animal model of congenital kyphoscoliosis will provide a basis for the treatment of this disease in humans. The present review aimed to introduce molecules and mechanisms associated with the pathogenesis of kyphoscoliosis and to discuss the usefulness of studying this disease using model rats that develop kyphoscoliosis.
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http://dx.doi.org/10.3892/etm.2024.12705 | DOI Listing |
Cureus
November 2024
Orthopedic Surgery, Universiti Putra Malaysia, Serdang, MYS.
Kyphoscoliosis is a spinal disorder where the spine's natural curvature is abnormally altered in multiple planes. It may be associated with the presence of a hemivertebrae, as discussed in this case. Negligence of this deformity may cause symptoms of back pain, worsening spinal deformity leading to reduced lung expansion, or neurological deficit impacting the quality of life for the worse.
View Article and Find Full Text PDFA A Pract
December 2024
From the Liverpool Hospital, Liverpool, New South Wales, Australia.
Pan Afr Med J
August 2024
Department of Respiratory Medicine, Datta Meghe Institute of Higher Education and Research, Wardha, Maharashtra, India.
Cureus
October 2024
Spine Surgery, Shiga General Hospital, Shiga, JPN.
There are few reports of syndromic scoliosis accompanied by a congenital vertebral anomaly. We report a case of Sotos syndrome with a concomitant congenital wedged vertebra whose kyphoscoliosis progressed rapidly and presented with myelopathy during the growth-spurt period. A 12-year-old male suffering from Sotos syndrome with T10-wedged vertebra presented with paraparesis and urinary dysfunction.
View Article and Find Full Text PDFChilds Nerv Syst
December 2024
Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India.
Purpose: To document the pre-operative rate of clinical deterioration in a cohort of patients with split cord malformation type 1 (SCM 1) and the early- and long-term surgical outcome in these patients.
Methods: Data from 41 patients with SCM 1 operated upon by the same surgeon (VR) between January 2008 to June 2023 were retrospectively reviewed with respect to history of clinical deterioration prior to surgery and early and long-term surgical outcomes.
Results: The mean age of the patients at presentation was 79.
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