abstract how to cite this article: akhondian j, ashrafzadeh f, beiraghi toosi m, moazen n, mohammadpoor t, karimi r. joubert syndrome in three children in a family: a case series. iran j child neurol. 2013 winter: 7(1); 39-42.   joubert  syndrome  (js)  is  a  rare  autosomal  recessive  central  nervous system malformation characterized by hypoplasia of the cerebellar vermis, hypotonia and abn...

abdominal compartment syndrome is a dangerous clinical situation, usually following abdominal injuries &operations.; it is seldom observed in patients with gynecologic and obstetric problems. abdominal compartment syndrome may be consequence ovarian hyperstimulation syndrome. a 28-year-old woman presented as a sever ovarian hyperstimulation.the increased iap indicated that ohss may be considere...

Background: Behcet’s disease is a recurrent, chronic and multi-systemic disease, which is determined by mucocutaneous manifestations. It spreads all over the world. The most common areas are in the Middle East, Mediterranean and Far East. Objective: The aim of this study was to determine the frequency of clinical manifestations of Behcet’s disease in patients admitted to dermatology ward ...

background : the metabolic syndrome has known as an independent risk factor of stroke. the occurrence of this syndrome is due to genetic factors and lifestyle. this study was performed   on the frequency of metabolic syndrome prevalence in ischemic stroke patients compare to control. methods : one hundred ischemic stroke patients and 100 controls (with the same age and sex) were evaluated for t...

background : lifestyle is recognized as a key factor as the cause and management of the metabolic syndrome. the aim of this study was to identify individuals at increased cardiovascular diseases risk and determine main features of lifestyle of participants with metabolic syndrome via internet. methods : the study was conducted from jun 22 to august 22, 2012 in tehran, iran. recruitment was carr...

apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. we present an atypical phenotype of this syndrome with right sided unilateral coronal synostosis. however, type i apert hand and other clinical and radiological features suggestthe diagnosis. genetic analysis revealed an absence of ...

kindler's syndrome is a rare entity of unknown cause characterized by acral blisters early in life followed by progressive diffuse poikiloderma and cutaneous atrophy. the inheritance pattern of this syndrome is not clear. we report four iranian siblings (three boys and one girl) with this syndrome, who were the result of a consanguineous marriage. in addition to the usual manifestations of the ...