background and aims: depression disorder is one of the most common diseases, but the diagnosis is widely complicated and controversial because of interventions, overlapping and confusing nature of the disease. so, keeping previous patients’ profile seems effective for diagnosis and treatment of present patients. use of this memory is latent in synthetic neuro-fuzzy algorithm. present article in...

Introduction Behçet’s disease (BD) is a vasculitis in which the hallmark lesions are oral and often genital ulcers. Involvement of parenchymal central nervous system (neuro-Behçet’s) is a serious complication commonly characterized by brainstem and/or basal ganglia lesions. To date, treatment of neuro-Behçet’s remains largely empirical, and may not adequately control the disease (1). Serum tumo...

Behçet's disease (BD) is an immuno-inflammatory multi-systemic characterized by ophthalmological and skin involvement, also oral genital ulcers. Its etiology pathogenesis are not clearly known. Neuro-Behçet's can occur as isolated form or a rare complication of BD. Besides, diagnosis neuro-Behçet's difficult. Since Neuro-Behçet result in morbidity mortality, early treatment important. The most ...

Behçet's disease (BD) was described as a three-symptom complex comprising uveitis, oral aphthae, and genital ulcerations. It is a multisystemic, recurrent, inflammatory disorder and it is of unknown cause. Neuro-Behçet (NB) is present in 5%-7% of BD. Movement disorders have rarely been reported in NB. Here, we report a case of chronic parenchymal NB presenting with chorea.

This review highlights the diagnostic criteria and neuro-ophthalmic symptoms and signs of the more commonly seen neurocutaneous disorders, including NF1 and NF2, tuberous sclerosis, VHL disease, Sturge-Weber disease, and AT. The distinct neuro-ophthalmic features in each of these hereditary and congenital disorders play an important role in clinical diagnosis.

Incontinentia pigmenti (IP) is an uncommon X-linked dominant multisystem disorder, lethal in the majority of affected males in utero and variably expressed in females. The cutaneous manifestations are diagnostic and classically occur in four stages: vesicular, verrucous, hyperpigmented, and atrophic. The skin lesions are typically spread along the lines of Blaschko, and they are usually present...

Citation: New PZ and Rosenfeld MR (2017) Editorial: Pitfalls in the Neuro-Imaging of Glioblastoma in the Era of Antiangiogenic and Immune-Targeted Therapy—Detecting Elusive Disease, Defining Response. Front. Neurol. 8:311. doi: 10.3389/fneur.2017.00311 Editorial: Pitfalls in the Neuro-imaging of Glioblastoma in the Era of antiangiogenic and immune-targeted therapy—detecting Elusive disease, def...

OBJECTIVE Canavan's disease is a lethal illness caused by a single gene mutation that is inherited as an autosomal recessive pattern. It has many different clinical features especially in the non-Ashkenazi Jewish population. MATERIAL & METHODS 45 patients were referred to the Pediatric Neurology Department of Mofid Children's Hospital in Tehran-Iran from 2010-2014 with a chief complaint of ne...