000			02018nam a22002537a 4500
001			R000791
003			PILC
005			20241111151527.0
008			241111b |||||||| |||| 00| 0 eng d
040			_beng _cFEU-NRMF MEDICAL LIBRARY _drda
050			_aMED 2024 0010
245			_aA 57-year-old male with Pharyngeal-Cervical-Brachial variant of Guillain-Barre Syndrome: A case report / _b[author]: Natasha Elaine L. Pecache,
260			_aFairview, Quezon city; _bDepartment of Internal Medicine, FEU-NRMF, _c2024
300			_c( in folder) _ewith flash drive (soft copy)
336			_2rdacontent _atext
337			_2rdamedia _aunmediated
338			_2rdacarrier _avolume
504			_aIncludes bibliographical references
520			_aABSTRACT Guillain-Barre syndrome (GBS) is an acute, rare, frequently severe, and fulminant post-infectious polyradiculoneuropathy that is autoimmune in nature. It results from the autoimmune destruction of nerves in the peripheral nervous system causing symptoms such as numbness, tingling, and weakness that can progress to paralysis. In this report, we describe an adult man who consulted due to severe headache, odynophagia, dysphagia, dysarthria, loss of balance, ophthalmalgia, blurring of vision, and bilateral ptosis. During the course of his admission, he had symptoms of persistent headache, dysphagia, dysarthria, complete 3rd nerve palsy, and upper limb weakness. Further workup confirmed that he has a sensorimotor, primarily demyelinating, polyneuropathy leading to a diagnosis of Guillain Barre’ Syndrome should be a standard in patients who present with polyneuropathy. Early recognition and diagnosis will guide us to the proper management and help improve the patient and their family’s quality of time.
521			_aRESDM
700			_aNatasha Elaine L. Pecache _eauthor
856			_21 _30 _qpdf _uhttps://library.feu-nrmf.ph/cgi-bin/koha/opac-retrieve-file.pl?id=8bda54e22a77074c9b3e3906533de2c0 _yClick here for FULL TEXT _1ALL
942			_2lcc _cRE
999			_c13221 _d13221