Acute motor and sensory axonal neuropathy

A rare motor-sensory, axonal form of Guillain-Barré syndrome (GBS).



Input patient's signs and symptoms


Narrow down the case reports



Total: 20 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(35.3%)
28930847
(5617714)
Guillain-Barre-like axonal polyneuropathy associated with Toscana virus infection: A case report.
Rota E, Morelli N, Immovilli P, De Mitri P, Guidetti D.
Medicine (Baltimore). 2017;96(38):e8081.
Facial diplegia
Adult Bunyaviridae Infections Guillain-Barre Syndrome Homo sapiens Male Paresthesia Sandfly fever Naples virus
1
(35.3%)
12365564
Postvaccinal inflammatory neuropathy: peripheral nerve biopsy in 3 cases.
Vital C, Vital A, Gbikpi-Benissan G, Longy-Boursier M, Climas MT, Castaing Y, Canron MH, Le Bras M, Petry K.
J Peripher Nerv Syst. 2002;7(3):163-7.
Facial paralysis
CSF2
Adult Biopsy Females Hepatitis B Vaccines Homo sapiens Inflammation Male Myelin Sheath Peripheral Nervous System Diseases Polyneuropathy
3
(24.9%)
29961501
A 2-Year-Old Boy With Difficulty Waking After Bone Marrow Transplantation.
Broomall E, Taylor JM, Peariso K.
Semin Pediatr Neurol. 2018;26:120-123.
Polyneuropathy Nuchal rigidity
Bone Marrow Transplantation Child, Preschool Differential Diagnosis Guillain-Barre Syndrome Homo sapiens Immunotherapy Male Movement Disorders Postoperative Complications Wiskott-Aldrich Syndrome
4
(17.5%)
24330286
Transverse myelitis and acute motor sensory axonal neuropathy due to Legionella pneumophila: a case report.
Canpolat M, Kumandas S, Yikilmaz A, Gumus H, Koseoglu E, Poyrazoglu HG, Kose M, Per H.
Pediatr Int. 2013;55(6):778-82.
Muscle weakness
Child Females Guillain-Barre Syndrome Homo sapiens Legionnaires' Disease Myelitis, Transverse
4
(17.5%)
16138251
Acute motor and sensory axonal neuropathy (AMSAN) in a 15-year-old boy presenting with severe pain and distal muscle weakness.
Rostasy KM, Huppke P, Beckers B, Brockmann K, Degenhardt V, Wesche B, Konig F, Gartner J.
Neuropediatrics. 2005;36(4):260-4.
Muscle weakness
Axon CD8 Antigens Guillain-Barre Syndrome Hepatitis A Virus Cellular Receptor 1 Homo sapiens Immunohistochemistry Male Membrane Glycoproteins Muscle Weakness Neurologic Examination Pain Receptors, Virus Transmission Electron Microscopy
6
(4.0%)
31198762
Guillain Barre syndrome with pulmonary tuberculosis: A case series from a tertiary care hospital.
Malakar S, Sharma TD, Raina S, Sharma KN, Kapoor D.
J Family Med Prim Care. 2019;8(5):1794-1797.
Polyneuropathy
6
(4.0%)
30642853
Fulminant Guillain-Barre syndrome in a patient with systemic lupus erythematosus.
Coomes EA, Haghbayan H, Spring J, Mehta S.
BMJ Case Rep. 2019;12(1):.
Nephritis
Electromyography Glucocorticoids Guillain-Barre Syndrome Homo sapiens Lupus Erythematosus, Systemic Lupus Nephritis Male Middle Aged Plasmapheresis
6
(4.0%)
30335268
Acute motor and sensory axonal neuropathy associated with Sjogren's syndrome.
Ethemoglu O , Kocaturk O , Zeynep E .
Ideggyogy Sz. 2018;71(9-10):352-356.
Sensory axonal neuropathy
Adrenal Cortex Hormones Adult Axon Females Guillain-Barre Syndrome Homo sapiens Motor Neurons Peripheral Nervous System Diseases Sjogren's Syndrome
6
(4.0%)
30159189
(6109579)
A Rare Axonal Variant of Guillain-Barre Syndrome following Elective Spinal Surgery.
Dowling JR, Dowling TJ Jr.
Case Rep Orthop. 2018;2018:2384969.
Respiratory tract infection
6
(4.0%)
30031375
(6054855)
Miller Fisher syndrome, Bickerstaff brainstem encephalitis and Guillain-Barre syndrome overlap with persistent non-demyelinating conduction blocks: a case report.
Puma A, Benoit J, Sacconi S, Uncini A.
BMC Neurol. 2018;18(1):101.
Ophthalmoplegia
CST7
Encephalitis Guillain-Barre Syndrome Homo sapiens Male Middle Aged Miller Fisher Syndrome
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 9

HPO ID Term # of case reports
HP:0001271 Polyneuropathy 1
HP:0001298 Encephalopathy 1
HP:0001347 Hyperreflexia 1
HP:0001701 Pericarditis 1
HP:0002202 Pleural effusion 1
HP:0002861 Melanoma 1
HP:0012115 Hepatitis 1
HP:0012246 Oculomotor nerve palsy 1
HP:0100721 Mediastinal lymphadenopathy 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID