مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
Title: 
Author(s): 

Issue Info: 
  • Year: 

    0
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    -
Measures: 
  • Citations: 

    0
  • Views: 

    5381
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Title: 
Author(s): 

Issue Info: 
  • Year: 

    0
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    -
Measures: 
  • Citations: 

    0
  • Views: 

    3435
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 3435

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Title: 
Author(s): 

Issue Info: 
  • Year: 

    0
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    -
Measures: 
  • Citations: 

    0
  • Views: 

    1532
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 1532

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Issue Info: 
  • Year: 

    1381
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    54-57
Measures: 
  • Citations: 

    0
  • Views: 

    1436
  • Downloads: 

    0
Abstract: 

سندرم کورنلیا دلانگه یک بیماری ژنتیکی است. توارث اتوزومال بارز و نهفته و گاهی همراه با برخی ناهنجاری های ساختمانی کروموزمی در این بیماری شناخته شده است. ولی بیشتر موارد آن به صورت جهش بارز بوده است. طول عمر افراد مبتلا کم است، تعداد زیادی از آنها در دوره نوزادی و کودکی می میرند. فراوانی این بیماری یک مورد در صد و پنجاه هزار تولد تخمین زده می شود.در این مقاله یک دختربچه 7 ساله مبتلا به این بیماری گزارش شده است. به جز پرمویی بدن، کلیه علایم ویژه این بیماری یعنی پایین بودن خط رویش مو در پس سر، ابروان پرپشت و به هم چسبیده، بینی باریک سربالا، کوتاهی قد و همچنین دست ها و پاهای کوتاه در این کودک وجود داشتند.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

MOHAMMADI M.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    3-8
Measures: 
  • Citations: 

    0
  • Views: 

    897
  • Downloads: 

    0
Abstract: 

How could we actually find the answers to our every day"s practice queries information overload ? We could find the answers thanks to Evidence Based Practice (EBM) .In the following review article I have tried to illustrate an EBM model of approach to one of the greatest concerns of every day practice of pediatricians (i.e. seizure and fever and febrile seizure). After a case presentation , I have Listed some common questions of every day"s practice ; then I have tried to find the answers through common and well-Known medical information data systems . After finding the relevant data and researches in literature and doing on them , I have Listed some evidence based recommendations .

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    9-12
Measures: 
  • Citations: 

    0
  • Views: 

    3718
  • Downloads: 

    0
Abstract: 

Malignances are most frequent causes of mortality in children aged 1-16 years. In an epidemiologic study, all cases of pediatric cancer (aged 1-16 years) registered by the Medical Universities in Iran are studied regarding the age, sex and type of malignancy. This study refers to the cancer diagnosed and histopathologically confirmed in 1996.Of the data received from 9 Provinces, a frequency of cancer in 420 children (58.3% male, 41.7% female) with a median age of 7.1 years was established. Hematologic malignancies with 20% of all cases were the most frequently encountered censer types. The next cases consisted of brain (15%), lymph nodes (15%), bone (8%), Kidney (7%), ophthalmic (6%), and (5%) malignancies.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

DANESHJOU KH. | HADJIZADEH N.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    13-17
Measures: 
  • Citations: 

    2
  • Views: 

    2608
  • Downloads: 

    0
Abstract: 

The expanded global use of Vaccines has led to eradication of some contagious diseases in children .This should not lead to forget the fact that these vaccines can be associated by complication and side effects. We studied 450 children, who had received DPT vaccine at the age of under 6 years. 2 to 7 days after the DPT injection we could not observe any seriously dangerous complication, although 82.4% of children had general and 83% local complications. Fever with a frequently observed general complication, this was following by lethargy, loss of appetite, persisted crying.The most frequently observed local complication consisted of pain at the site of injection with 63% of cases followed by swelling, erythema and in duration.By increasing age, local swelling and erythema (P<0.001) and induration decreases (P<0.001). General complications decrease with age and vaccinations, which especially remarkable in 2 to 7 year old children (5 th vaccination).

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

HAGSHENAS Z.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    18-20
Measures: 
  • Citations: 

    0
  • Views: 

    1340
  • Downloads: 

    0
Abstract: 

Cystic fibrosis (CF) is an inherited multisystem disorder of children and adult. Characterized chiefly by chronic obstruction infection of airways, maldigestion and its consequences. It is the most life limiting recessive genetic trait among whites. A dysfunction of epithelial surfaces is the predominant pathogenic feature and is responsible for a broad, variable and sometimes confusing array of presenting manifestation and complications.This article present an about 11-month old infant who was hospitalized because and hyponatremia of unknown origin. In the third hospitalization a CF was diagnosed. CF treatment lead to resolving of hyponatremia and convulsions.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

AKHOUNDIAN J.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    21-25
Measures: 
  • Citations: 

    0
  • Views: 

    1596
  • Downloads: 

    0
Abstract: 

Epilepsy occurs in 15-60% of children with cerebral palsy (CP). However, its clinical course is not well defined. This retrospective study reviews the prevalence, nature and prognosis of epilepsy in cerebral palsy. 53 of 133 children with cerebral palsy seen in the Neuropediatric Clinic in Mashhad, emam Reza Hospital between 1999 and 2001 had epilepsy.A control group of 70 epileptic children with normal neurodevelopment status was seen during the same period.Epilepsy most commonly affected patients with spastic quadriplegia. when compared with controls, children with cerebral palsy had higher incidence of epilepsy with onset within the first year of age (52.8% vs 18.5%), a history of neonatal seizures (20.7% vs 4.2%) polytherapy (76.3%vs 29.1%) and treatment with the second line antiepileptic drugs (79.2% vs 23.1% ). Thus epilepsy is common in children with CP and the use of new antiepileptic drugs and surgical treatment might eventually improve both seizure control and of in life in epileptic children with CP.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

GHOFRANI M.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    26-28
Measures: 
  • Citations: 

    0
  • Views: 

    2245
  • Downloads: 

    0
Abstract: 

Urinary and rectal sphincter incontinence is a frequently encountered symptom in mentally retarded children and those with learning disabilities.In addition to the fact that incontinence is a very disagreeable problem, on the whde it is of more importance in Islamic societies, as to be "clean" during religious practices is mandatory.Regarding the fact that 25-50 percent of mentally retarded children are unable to control urine and faces elimination, families and institutions in charge of these children face much inconvenience. This article discusses the teaching programs and methods of behavioral therapy of the affected patients.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

ASHRAFI M.R. | GHOFRANI M.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    29-34
Measures: 
  • Citations: 

    0
  • Views: 

    5555
  • Downloads: 

    0
Keywords: 
Abstract: 

Chloride channel myotonia is a form of channelopathy, and myotonia is its main manifestation. Myotonia my be defined as delayed relaxation of skeletal muscle after its contraction. Decreased chloride conductance across the transverse tubular system, renders the muscle membrane hyper excitable and leads to repetitive firing, creating myotonia. Myotonia congenita is another name for chloride channel myotonia. Myotonia congentia appears in autosomal dominant type called Thomsen disease, autosomal recessive type called Becker disease, and a type with sporadic occurrence.Symptoms appear in the first or second decade of life. Repeated muscle contractions, the so called warm up, result in resolution of the myotonia stiffness. Muscles stiffness and hypertrophy is another finding at physical examination In this study we report on five patients, which had clinical and electrical signs of myotonia. Muscle hypertrophy and warm up phenomena were present in all cases. CPK measurement of all cases were normal. Two patients underwent muscle biopsy that showed only atrophy increased central nuclei. In three cases autosomal recessive inheritance (Becker), in one case autosomal dominant inheritance (Thomsen) and in one case sporadic occurrence was suggested. With respect to successful results of carbamazepine therapy in 4 patients, and being excellent in one of them, we suggest carbamazepine for the first choice of myotonia treatment.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

SHARIFI F.A.S.

Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    35-38
Measures: 
  • Citations: 

    1
  • Views: 

    1076
  • Downloads: 

    0
Abstract: 

Mothers' lack of knowledge of supplementary nutrition in 6-12 months old children is an important element causing dyfunction in child nutrition in this period of life and as a result leads to malnutrition and contributes to the high infant mortality. The aim of this research was to determine mothers' knowledge of child supplementary nutrition in Babol city and the surrounding villages.This is a descriptive and analytic Study. The information was gathered by questionnaires completed by 190 mothers in villages around Babol.The average knowledge of mothers in the rural region was good. Mothers who were 25-29 years old, had an optimum level of knowledge. Working mother were more informed than non-working mothers.Mothers with more than three children had less knowledge than mothers with only one child. 84.7 percent used to feed supplementary food at 6th month.Mothers living in the rural region had suitable degree of knowledge regarding the supplementary nutrition. 91 peresent of mothers living in rural region had a knowledge of more than the level. The results of this research are similar to those of other region of Iran and also other developing countries. It was shown that there are some factors playing a role in mothers' knowledge to supplementary nutrition such as the level of education, availability of health houses, and the information provided by media. However, it seems that with training of the health care workers and with more assistance of the media the mothers" knowledge regarding supplementary nutrition can improved.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    40-44
Measures: 
  • Citations: 

    0
  • Views: 

    706
  • Downloads: 

    0
Abstract: 

Progressive pseudorheumatoid chondrodysplasiais a rare disorder. Signs and symptoms of the disease develop between three and eight years of age.Patients show clinically and radio graphically continued cartilage ioss and destructive bone changes as they age. In this article we report on a 6-year old boy who had been referred to our Neuropediatric clinic for neuromuscular survey.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 706

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Issue Info: 
  • Year: 

    2002
  • Volume: 

    12
  • Issue: 

    3
  • Pages: 

    45-48
Measures: 
  • Citations: 

    0
  • Views: 

    1153
  • Downloads: 

    0
Abstract: 

This prospective study was conducted to observe changes in nasopharyngeal (NP) pneumococcal carriage within 4 to 5 days after initiation used antibiotics of commonly used antibiotics for 150 patients who were admitted at Infectious Disease Unit of children's Medical Center in Tehran to determine whether a significant increase in the carriage rate of drug (penicillin) resistant S. pneumonia on NP can be observed within this short interval.Nasopharyngeal culture for s. pneumonia was obtained before (Day 1) and after (Day 4 to 5) initiation of antibiotic treatment. Antibiogram was performed in all isolates and the MIC of penicillin in 20 resistant S. pneumonia. by E-test Among initial 46 (30%) pneumococcal isolates 28 (60%) were sensitive and 8 (17%) were resistant to penicillin.After 4 to 5 days of antibiotic treatment with various drugs, 20 (13%) pneumococcal isolates in the culture were obtained. of whom 12 patients (60%) were resistant to penicillin and 8 patients (40%) were sensitive. In 4 of 150 patients (2.6%) a new S. pneumoniae isolate was recovered 4 to 5 days after initiation. All of those isolates were penicillin-resistant.conclusion: a rapid detection of penicillin - nonsusceptible NP pneumonia isolates during antibiotic treatment is common. This may contribute to the spread of resistant pneumococci.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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