Creutzfeld -Jacob Disease (CJD) is a rare type of neurodegenerative disease caused due to prion disease and is rapidly progressive and fatal. It is usually suspected based on the typical presenting symptoms, most important symptom being rapidly progressive dementia. Cases with atypical presentation are usually missed due to low clinical suspicion.
We present a case report of a 64-year-old male who presented with worsening cerebellar ataxia and only mild dementia.MRI done to rule out any organic cause, revealed classic findings of CJD.Following this EEG was performed. MRI helped in clinching the diagnosis in this case of low clinical suspicion. This was an extremely rare variant of CJD-the brownell openheimer variant.(1)
Partial tentorial hypoplasia with ipsilateral focal brain herniation is an extremely rare cause of idiopathic intracranial herniation with very few
cases reported in the literature. This is an essentially benign condition which may mimic a sinister pathology to a radiologist unaware of this rare
entity.We present a case of 58 year old male presenting with giddiness and headaches. An MRI brain was performed which revealed this rare
incidental nding which on the rst look simulated a mass.
To improve the efficiency of the management of college stadiums and gymnasiums, an information management system for college gymnasium was developed. In the information management system of university gymnasium, the integration of management functions was realized, including employee management, customer management, site management, cost management and system management. The system integrated all these functions in the system and realized the transmission and sharing of data and information. The system also optimized the overall process of the college gymnasium information management system and realized the goal of the open management of the daily information of the college gymnasium. Moreover, the system could make use of its open interface to integrate the management system with other colleges and universities. The research showed that the information management system of university gymnasium improved the efficiency of the management of sports stadium and gymnasium. In a word, it has practical application value in the management of college gymnasium.
Androgen insensitivity syndrome (AIS), also known as testicular feminization, an X-linked recessive disorder comprises a wide range of phenotypes that are caused by various types of mutations in the androgen receptor gene. AIs can be classified as complete, partial, or mild based on the phenotypic presentation. The clinical findings include a female type of external genitalia, 46-XY karyotype, absence of Mullerian structures, presence of Wolffian structures to various degree, and normal to high testosterone and gonadotropin levels. We report this case as an interesting and rare syndrome. The patient is a 15-year-old phenotypic female who presented with primary amenorrhea and normal-appearing external genitalia. Orchidectomy was done after proper counselling and proper psychological support was given to her.
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