Clinico-Radiological Findings of Neuro-Behcet's Syndrome.
نویسندگان
چکیده
منابع مشابه
[Radiological findings in Currarino syndrome].
OBJECTIVE To describe the clinical, radiological and genetic findings of a family affected by Currarino syndrome (CS) (agenesis of the sacrum, presacral mass, and anal-rectal anomalies), and to familiarise the radiologist with this condition that, although uncommon, could be suspected by its characteristic images. MATERIAL AND METHODS A study was made of 8 out of 9 family members (the parents...
متن کاملRadiological findings in Wolfram syndrome.
OBJECTIVE To determine the precise radiologic findings in Wolfram syndrome (WFS) patients using objective techniques in order to better define the reference population for the clinical evaluation. METHODS Sixteen patients (6 males and 10 females) with WFS found in 4 families were included in this study. Fourteen patients with WFS-2 came from 3 families while 2 patients with WFS-1 from one fam...
متن کاملAarskog-Scott Syndrome: Clinico-Radiological Illustration of a Rare Case
Aarskog-Scott Syndrome is a rare syndrome and is estimated to occur in 1 in 1 million individuals in general population. It is transmitted in an X-linked recessive manner and occurs due to FGD1 gene mutation. It has facial, genital and digital hands symptoms, musculoskeletal anomalies and affected growth. Here we present a case of Aarskog-Scott syndrome in an 18-year-old male patient with the c...
متن کاملClinico-radiological correlation of nutcracker syndrome: a single centre experience.
The term nutcracker syndrome (NS) refers to the compression of left renal vein between the aorta and the superior mesenteric artery (SMA) causing renal venous hypertension. The symptoms vary from asymptomatic hematuria to severe pelvic congestion. The purpose of this study is to evaluate the clinical characteristics of patients with NS and the correlation between clinical and laboratory finding...
متن کاملMiddle aortic syndrome: clinical and radiological findings.
Eight patients with the middle aortic syndrome are described. They were aged 2 months to 14 years at diagnosis; follow up was one to 11 years. Clinical presentations included asymptomatic hypertension (n = 5), severe headache, nose bleed, and chest pain (n = 1), and cardiac failure (n = 1). All had severe hypertension requiring multiple drug treatment. Diminished peripheral pulses were not help...
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ژورنال
عنوان ژورنال: Internal Medicine
سال: 1994
ISSN: 0918-2918,1349-7235
DOI: 10.2169/internalmedicine.33.136