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Relevant bibliographies by topics / Congenital absence of unilateral zygapophyseal joint

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Academic literature on the topic 'Congenital absence of unilateral zygapophyseal joint'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Congenital absence of unilateral zygapophyseal joint"

1

Adsul, Nitin Maruti, Manoj Kumar, Shankar Acharya, K. L. Kalra, and R. S. Chahal. "Congenital absence of a lumbosacral facet joint: A case report." Surgical Neurology International 11 (January 24, 2020): 15. http://dx.doi.org/10.25259/sni_606_2019.

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Background: Congenital absence of the lumbosacral facet joint is extremely rare, with only 26 cases reported in the literature. Here, we present a patient with the unilateral absence of the left fifth lumbar inferior articular process and reviewed the relevant literature. Case Description: A 32-year-old gentleman, who had undergone right L4-5 lumbar microdiscectomy 3 months ago now presented with acute low back and left leg pain following a fall. He is now presented with acute low back and left leg pain following a fall. Plain radiographs of the L-S spine revealed an absent left L5–S1 zygapoph

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2

International, Journal of Medical Science and Innovative Research (IJMSIR). "Congenital Absence of Unilateral Zygapophyseal Joint and S1 Superior Articular Facet in An Adult Patient – A Case Report." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 4 (2024): 01–03. https://doi.org/10.5281/zenodo.15424123.

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<strong>Abstract</strong> This case report describes a rare congenital absence of the L5-S1 lumbosacral articular facet joint and S1 superior articular facet on the left side in a 17-year-old male presenting with lower back pain. Despite being asymptomatic in most cases, this anomaly was diagnosed through a CT scan, highlighting the importance of advanced imaging for accurate diagnosis. Awareness of such rare congenital defects is crucial for proper management of unexplained lower back pain.

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3

Maalouly, Joseph, Dany Aouad, Hicham G. Abd El Nour, Alexandre Nehme, and Fouad Jabbour. "Isolated Congenital Absence of Lumbosacral Facet Joint." Case Reports in Orthopedics 2019 (February 12, 2019): 1–3. http://dx.doi.org/10.1155/2019/1465460.

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A congenital absence of the lumbar facet joint is a rare reported condition. This is the case of a 32-year-old male patient presenting with severe low back pain radiating to his right lower limb. Physical examination revealed no motor deficits, but right lower limb numbness was reported over dorsum aspect of the right foot. No other sensory or motor disturbances were reported or found on exam. Imaging studies, consisting of a spine MRI and spine CT scan with 3D reconstruction, revealed the absence of the right L5-S1 zygapophyseal joint. The patient was treated conservatively with resolution of

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4

Kumar, S., R. Baidya, and P. Baral. "A Rare Anomaly of the Long Head of the Biceps Brachii Muscle." Journal of Gandaki Medical College-Nepal 11, no. 1 (2018): 56–57. http://dx.doi.org/10.3126/jgmcn.v11i1.20796.

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Introduction: Biceps brachii is a muscle of arm which brings about supination when fore-arm is flexed and flexion of elbow joint. Proximally it is attached with two heads: long and short heads.Case report: The absence of long head of biceps brachii muscle is very rare anomaly. It may be unilateral or bilateral with or without other congenital anomalies. The exact prevalence of this anomaly is unknown. This anomaly has been reported to occur as the result of an insult to the fetus during the sixth or seventh week of gestation, at which time the long head of the biceps tendon is developing. J-GM

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5

Taves, Sarah, Junjiang Sun, Eric W. Livingston, et al. "Hemophilia A and B mice, but not VWF−/−mice, display bone defects in congenital development and remodeling after injury." Scientific Reports 9, no. 1 (2019). http://dx.doi.org/10.1038/s41598-019-50787-9.

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Abstract While joint damage is the primary co-morbidity of hemophilia, osteoporosis and osteopenia are also observed. Coagulation factor VIII deficient (FVIII−/−) mice develop an osteoporotic phenotype in the absence of induced hemarthrosis that is exacerbated two weeks after an induced joint injury. Here we have compared comprehensively the bone health of clotting factor VIII, factor IX, and Von Willebrand Factor knockout (FVIII−/−, FIX−/−, and VWF−/− respectively) mice both in the absence of joint hemorrhage and following induced joint injury. We found FVIII−/− and FIX−/− mice, but not VWF−/

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6

Sharma, Abhinav Kumar, and Abdikayimova Gulzat. "Ataxia By Abdikayimova Gulzat." March 23, 2025. https://doi.org/10.5281/zenodo.15073092.

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<strong>Article on ataxia – classification and management</strong> <em>Abhinav Kumar Sharma</em>   Under the guidance of <em>Abdikyimova G</em><em>ulzat Mam (Faculty of Neurology)</em> Professor - Osh State University,  IMF  Kyrgyzstan    <strong>Abstract</strong> <em>Ataxia has been described as incoordination of voluntary movements and abnormal postural control. There are many different statements concerning the definition, range and nomenclature of ataxia. Different clinical findings, exposure to different neurological structures and different causes lead to t

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