Motor Axonal Neuropathy Associated With Idiopathic CD4+T-Lymphocytopenia
نویسندگان
چکیده
منابع مشابه
Motor Axonal Neuropathy Associated With Idiopathic CD4+ T-Lymphocytopenia
Idiopathic CD4(+) T-lymphocytopenia is a rare immune disorder characterized by an unexplained deficit of CD4(+) T cells and results in various opportunistic infections. Herein, we report a case of new onset weakness in a 10-year-old boy secondary to motor axonal neuropathy associated with idiopathic CD4(+) T-lymphocytopenia. The patient was referred to rehabilitation for an evaluation of progre...
متن کاملAcute motor axonal neuropathy
By Sameera Salman Ghauri (Dr. Ghauri of University of Texas Houston Health Science Center has no relevant financial relationships to disclose.) Suur Biliciler MD (Dr. Biliciler of University of Texas Houston Health Science Center has no relevant financial relationships to disclose.) Thy Nguyen MD (Dr. Nguyen of University of Texas Health Science Center has no relevant financial relationships to...
متن کاملAntiretroviral Therapy-Associated Acute Motor and Sensory Axonal Neuropathy
Guillain-Barré syndrome (GBS) has been reported in HIV-infected patients in association with the immune reconstitution syndrome whose symptoms can be mimicked by highly active antiretroviral therapy (HAART)-mediated mitochondrial toxicity. We report a case of a 17-year-old, HIV-infected patient on HAART with a normal CD4 count and undetectable viral load, presenting with acute lower extremity w...
متن کاملConduction block in acute motor axonal neuropathy.
Guillain-Barré syndrome is divided into two major subtypes, acute inflammatory demyelinating polyneuropathy and acute motor axonal neuropathy. The characteristic electrophysiological features of acute motor axonal neuropathy are reduced amplitude or absence of distal compound muscle action potentials indicating axonal degeneration. In contrast, autopsy study results show early nodal changes in ...
متن کاملSevere Pure Acute Motor Axonal Neuropathy
Acute motor axonal neuropathy (AMAN) is a subtype of Guillain–Barré syndrome. Characteristic electrophysiological features of AMAN are reduced amplitude or absence of muscle action potentials. Our patient described progressive weakness in his leg and was not able to independently walk; he had a feeling weakness in his arms within 24 h after the onset of symptoms. He was diagnosed with AMAN acco...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Annals of Rehabilitation Medicine
سال: 2013
ISSN: 2234-0645,2234-0653
DOI: 10.5535/arm.2013.37.1.127