نتایج جستجو برای: congenital hydrocephalus
تعداد نتایج: 126851 فیلتر نتایج به سال:
This paper reports the experiences of the second clinical trial in the use of isosorbide in the treatment of 34 selected cases of infantile hydrocephalus of all types. Subject to careful biochemical monitoring of serum electrolyte, urea, and acid-base balance, treatment with 2 g/kg body weight 6-hourly is safe. Side effects are immediately eliminated by interrupting therapy. With lower dosage, ...
Haemangiomas are common, benign, vascular tumours, observed in 4-12% of infants during the first year of life. Most cases progress without complication, yet a small proportion experience life-threatening complications. Concomitant congenital malformations have been reported in a small but significant proportion of haemangioma patients. This study aimed to describe haemangioma cases and to ident...
Background: Hydrocephalus is a pathological brain disorder resulting from increased cerebrospinal fluid without or with elevated intracranial pressure in widening of the space where flows. Maternal environment such as experiencing infection during pregnancy, consuming alcohol and drugs, lifestyle obesity, diabetes, hypertension, lack examinations preparing for prenatal care low socioeconomic st...
Congenital hydrocephalus is considered as either acquired due to haemorrhage, infection or neoplasia or as of developmental nature and is divided into two subgroups, communicating and obstructive. Congenital hydrocephalus is either syndromic or non-syndromic, and in the latter no cause is found in more than half of the patients. In patients with isolated hydrocephalus, L1CAM mutations represent...
Modem surgical treatment of infantile hydrocephalus results in a significantly increased expectaon of life for patients so treated over those in --whom a conservative policy has been adopted. But in order to give as accurate a prognosis as possible, one must inquire whether the results bear any rdation to the aetiology of the condition. One of us (Guthkelch, 1967) has recently described his tec...
Introduction: Dandy Walker Syndrome (DWS) is a congenital brain malformation characterized by hypoplasia or absence of cerebellar vermis, cystic dilatation of fourth ventricle and hydrocephalus. It is frequently associated with other congenital anomalies. Associated central nervous system anomalies such as agenesis of corpus callosum and vermis are associated with poor prognosis. Association of...
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