Idiopathic Segmental Anhidrosis with Hyporeflexia: Incomplete Ross Syndrome
نویسندگان
چکیده
منابع مشابه
Segmental anhidrosis with hyporeflexia associated with congenital spinal deformity: a Ross's syndrome variant or inverse Horner's syndrome?
A 39-year-old soldier presented with anhidrosis affecting both upper extremities below the shoulders, the right side of the trunk below the third rib in front and the third vertebra on the back, and the left lower extremity below the inguinal ligament since 1992. Ten years later in 2002, he was also found to have bilateral absence of Achilles reflex and decreased right knee jerk. In addition, t...
متن کاملAnhidrosis as the first sign of Ross syndrome.
Resident in Dermatology, Federal Fluminense University, Antônio Pedro Hospital, Department of Dermatology, Niteroi RJ, Brazil; Resident in Neurology, Federal Fluminense University, Antônio Pedro Hospital, Department of Neurology, Niterói RJ, Brazil; Professor of the Dermatology Department, Federal Fluminense University, Antônio Pedro Hospital, Department of Dermatology, Niteroi RJ, Brazil; Chai...
متن کاملPRIMARY TORSION AND IDIOPATHIC SEGMENTAL INFARCTION OF OMENTUM
Torsion and infarction of the greater omentum are two rare clinical situations which present as an acute abdomen. Nevertheless, knowledge concerning these two problems can help the surgeon in proper diagnosis and treatment. Since the first report on primary torsion by Eitel in 1899, a few hundred more have been reported and some collective reviews published to date. In this study we will p...
متن کاملIdiopathic focal segmental glomerulosclerosis.
Idiopathic focal segmental glomerulosclerosis (FSGS) is a primary glomerular disease that essentially represents a form of chronic, progressive renal fibrosis for which there is no discernible cause. Often presenting with or eventually manifesting the nephrotic syndrome, this disease is increasing in incidence in both children and adults. Therapy continues to be a challenge, although some patie...
متن کاملIdiopathic Hypereosinophilic Syndrome
Idiopathic hypereosinophilic syndrome is a multisystem disease with peripheral blood eosinophilia of at least 6 months duration, multiple organ system involvement, and no evidence for other known causes of eosinophilia. It is characteristically a disease of middle-aged men, often has a poor prognosis and is seldom found during childhood. Heart dicsease, characterized by endomyocardial fibrosis ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of the Korean Neurological Association
سال: 2015
ISSN: 1225-7044,2288-985X
DOI: 10.17340/jkna.2015.4.20