A rare cause of femoral neuropathy: Giant cell tumor mimicking a femoral nerve sheath tumor [2026] - 398KB
by Vonny Fibrianty Goenawan, Vivien Puspitasari, Yee Wen Yong
Femoral neuropathy is an uncommon peripheral neuropathy typically caused by compression, trauma, or iatrogenic injury, while tumor-related involvement is rare. Giant cell tumors are mesenchymal lesion...

Late-diagnosed congenital myasthenic syndrome due to a CHRNE mutation: a case report [2026] - 463KB
by Pelin Yenilmez Yeşildaş, Nevra Öksüz
Congenital myasthenic syndromes (CMS) comprise a heterogeneous group of inherited disorders caused by genetic defects affecting neuromuscular junction transmission. Clinical manifestations range from ...

Co-occurrence of vitiligo and sweet ageusia in a post- thymectomy Myasthenia Gravis patient in remission: A case report [2026] - 554KB
by Mario B Prado Jr, Sofia Maria Im, Karen Joy B Adiao
While several journals have published the co-existence of dysgeusia or vitiligo with Myasthenia Gravis (MG), none had described their co-occurrence with MG. Moreover, they usually precede the incidenc...

From sarcopenia to a genetic diagnosis: Exercise- induced weakness and androgen insensitivity unmasking Kenedy’s disease [2026] - 448KB
by Kye Chiun Lau, Samihah Abdul Karim, Siew Li Goh, Mohamad Azwan Aziz
Spinal and bulbar muscular atrophy, or Kennedy’s disease, is a rare, X-linked neurodegenerative disorder often misdiagnosed due to its mimicry of common musculoskeletal conditions. Diagnostic delay ...

Contact lens-associated ocular allodynia in migraine: A case report highlighting peripheral sensory input in central sensitization [2026] - 283KB
by Devrimsel Harika Ertem
Allodynia, defined as the perception of pain from stimuli that are normally non-painful, is a hallmark of central sensitization in migraine pathophysiology. While cutaneous allodynia is well-documente...

Transient glabellar and diffuse facial erythema during migraine attacks: A rare autonomic manifestation [2026] - 608KB
by Gökhan Aydoğan, Fırat Uykur, Fuat Erdoğmuş, Gülnihal Kutlu Günergin
Migraine is a primary headache disorder frequently accompanied by cranial autonomic symptoms, and recent reports have described cutaneous phenomena such as the “red forehead dot” and glabellar ery...

Ultrasound-guided glossopharyngeal nerve block for glossopharyngeal neuropathy: Safe and easy to use [2026] - 1,188KB
by Oktay Faysal Tertemiz, Sinem Akkaya
A female patient who developed neuropathic pain in the left maxillary and left nasopharyngeal regions following a dental procedure was treated with carbamazepine, pregabalin, amitriptyline, and duloxe...

A rare neurological puzzle: Anti-Ma2 encephalitis linked to lung adenocarcinoma [2026] - 434KB
by Ceyhun Sayman, Merve Gözüaçık, Gökhan Gölle, Şeyda Çankaya, Burak Yuluğ
Anti-Ma2 encephalitis is a rare paraneoplastic syndrome, mainly associated with germ cell tumors of the testis. This case report represents an atypical presentation of anti-Ma2 encephalitis in a 65-ye...

When the mimic meets reality: AQP4-IgG seroconversion in a patient with profound biotinidase deficiency presenting with an NMOSD- like phenotype [2026] - 575KB
by Yavuz ATAŞ, Ünsal YILMAZ, Fehime ERDEM, Havva Akmaz ÜNLÜ, Perihan TUNÇ, Nihal SOYLU, Merve SOĞUKPINAR
Neuromyelitis optica spectrum disorder (NMOSD) is a chronic autoimmune inflammatory disease of the central nervous system. While aquaporin-4 immunoglobulin G (AQP4-IgG) antibodies are detected in most...

A rare cause of variant late-infantile neuronal ceroid lipofuscinosis: CLN8-related disease [2026] - 388KB
by Bhawna Sharma, Swati Garg, Shubham Agrawal, Aditi Jain
Neuronal Ceroid Lipofuscinosis (NCL) is a rare, inherited lysosomal storage disorder characterized by the accumulation of lipofuscin within neuronal cells, leading to progressive neurodegeneration. It...