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"Hee Won Lee"

Case Report
Sonographic Findings of Polyneuropathy Associated With Cerebrotendinous Xanthomatosis: A Case Report
Jung Yoon Yoon, Min-Wook Kim, Hyun Jung Do, Dae-Hyun Jang, Hee Won Lee
Ann Rehabil Med 2017;41(2):313-317.   Published online April 27, 2017
DOI: https://doi.org/10.5535/arm.2017.41.2.313

Cerebrotendinous xanthomatosis is a rare autosomal recessive disease that involves multiple organs, including the peripheral nervous system. The present study is the first to report the ultrasonographic findings of peripheral nerves in a patient with cerebrotendinous xanthomatosis. The patient presented with bilateral Achilles tendon enlargement and foot hypesthesia. Sonographic examination revealed hypoechoic, swollen peripheral nerves with enlarged bilateral Achilles tendons. Since the ultrasonographic findings revealed peripheral involvement, the diagnosis of cerebrotendinous xanthomatosis was established after laboratory and genetic studies along with clinical findings.

Citations

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  • Nerve Ultrasound Detects Peripheral Nerve Enlargement in Cerebrotendinous Xanthomatosis
    Antonio Edvan Camelo‐Filho, Pedro Lucas G. S. B. Lima, Tito B. S. Soares, Rodrigo Fagundes da Rosa, Luis Edmundo T. A. Furtado, Ana Lucila Moreira, André L. S. Pessoa, Paulo R. Nóbrega, Pedro Braga‐Neto
    Muscle & Nerve.2026;[Epub]     CrossRef
  • Polyneuropathy in Cerebrotendinous Xanthomatosis: Diagnostic Challenges and Potential for Therapeutic Intervention
    Antonio Edvan Camelo-Filho, Pedro Lucas Grangeiro Sá Barreto Lima, Francisco Luciano Honório Barreto Cavalcante, Oliver Reiks Miyajima, Carolina Figueiredo Santos, Rodrigo Fagundes da Rosa, André Luiz Santos Pessoa, Pedro Braga-Neto, Paulo Ribeiro Nóbrega
    Brain Sciences.2024; 14(11): 1159.     CrossRef
  • First case series of Polish patients with cerebrotendinous xanthomatosis and systematic review of cases from the 21st century
    Magdalena Badura‐Stronka, Adam Sebastian Hirschfeld, Anna Winczewska‐Wiktor, Edyta Budzyńska, Anna Jakubiuk‐Tomaszuk, Anita Piontek, Barbara Steinborn, Wojciech Kozubski
    Clinical Genetics.2022; 101(2): 190.     CrossRef
  • Myelin Defects in Niemann–Pick Type C Disease: Mechanisms and Possible Therapeutic Perspectives
    Antonietta Bernardo, Chiara De Nuccio, Sergio Visentin, Alberto Martire, Luisa Minghetti, Patrizia Popoli, Antonella Ferrante
    International Journal of Molecular Sciences.2021; 22(16): 8858.     CrossRef
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