Rohit Verma,Shivanand S Dalawayi
Rohit Verma
Suryanarayanan Bhaskar
Suryanarayanan Bhaskar
Authors' reply [0.03%]
作者答复
V V Ashraf,Nilesh V Chaudhary,R Praveen Kumar et al.
V V Ashraf et al.
Klinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's disease [0.03%]
伴有进行性脊髓性肌肉萎缩的克林菲elter综合征模拟肯尼迪病
Pedro Enrique Jiménez Caballero
Pedro Enrique Jiménez Caballero
Kennedy's disease, an X-linked spinal and bulbar muscular atrophy, is characterized by loss of lower motor neurons. Mild sensory deficits, gynecomastia and infertility may be observed. Klinefelter's syndrome is a variation of sex chromosome...
Painless orbital myositis [0.03%]
无痛性眼眶肌炎
Rahul T Chakor,N S Santhosh
Rahul T Chakor
Idiopathic orbital inflammation is the third most common orbital disease, following Graves orbitopathy and lymphoproliferative diseases. We present a 11 year old girl with 15 days history of painless diplopia. There was no history of fluctu...
S K Shankar,Anita Mahadevan,Silvano Dias Sapico et al.
S K Shankar et al.
We report a case of rabies viral encephalitis in a 48-year-old male with an unusually long incubation period, historically suspected to be more than 20 years. The case was referred for histological diagnosis following alleged medical neglig...
Cryptoccocal menigitis as a primary manifestation in a patient with intestinal lymphangictasia [0.03%]
肠淋巴管扩张症患者出现新型隐球菌脑膜炎
Shaik Afshan Jabeen,Aruna Murthy,Rukmini Mridula Kandadai et al.
Shaik Afshan Jabeen et al.
Opportunistic infections usually occur in patients with an immunocompromised state, and can be severe. Cryptoccocal meningitis is a fatal condition if left untreated, and is usually found in such patients. We report the case of an adult pat...
Megalencephalic leukoencephalopathy with subcortical cysts in all three siblings of a non-Aggarwal Indian family [0.03%]
非阿格瓦尔印度家族中三名同胞的亚皮质囊性巨脑性白质病
Mani Kant Kumar,Brish Bhanu Singh
Mani Kant Kumar
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare neurodegenerative disease seen mainly in the Aggarwal community in India. It is characterized by early-onset macrocephaly with mild motor developmental delay, gradua...
Hip dysplasia associated with a hereditary sensorimotor polyneuropathy mimics a myopathic process [0.03%]
遗传感觉运动多神经病伴发的髋关节发育不良类似肌病过程
Mohammad Javad Hadianfard,Alireza Ashraf
Mohammad Javad Hadianfard
Some orthopedic complications have been reported in the hereditary neuropathies. However, the association of the hip dysplasia with this category of neuropathy is rarely recognized. We present a 13-year-old boy with the progressive weakness...