نتایج جستجو برای: congenital microgastria

تعداد نتایج: 120300  

Journal: :international journal of pediatrics 0
shilpa kalane division of neonatology, department of pediatrics, deenanath mangeshkar hospital, pune,maharashtra, india. rajan joshi deenanath mangeshkar hospital, pune, maharashtra, india. arti rajhans deenanath mangeshkar hospital, pune,maharashtra,india.

hyperpigmentation over face in a neonate is rare and the differentials for the same are also rare. congenital chickengunya, fungal and viral infections, drug rash are few differentials. chikungunya virus (chikv) infection manifesting in neonates is very rare. the prevalence of the entity was described only recently. we describe a neonate with hyperpigmentation on day 3 of life with stormy cours...

Journal: :journal of biostatistics and epidemiology 0
majid sadeghifar department of statistics, school of basic sciences, bu-ali sina university, hamadan, iran. maryam seyed-tabib department of biostatistics & epidemiology, school of public health, hamadan university of medical sciences, hamadan, iran. saiedeh haji-maghsoudi department of biostatistics & epidemiology, school of public health, hamadan university of medical sciences, hamadan, iran. kourosh noemani department of non-communicable disease, school of health, ahvaz jundishapur university of medical sciences, ahvaz, iran. fariba aalipur-byrgany department of non-communicable disease, school of health, ahvaz jundishapur university of medical sciences, ahvaz, iran.

background & aim: congenital hypothyroidism (ch) is one of the most common endocrine diseases and is a major cause of preventable mental retardation. early diagnosis of ch can help prevent future diseases. although time series techniques are often utilized to forecast future status, they are inadequate to deal with count data with overdispersion. the aim of this study was to apply poisson hidde...

Journal: :journal of basic research in medical sciences 0
kourosh sayehmiri university of medical sciences ilam mohammad reza kaffashian department of physiology, faculty of medicine, ilam university of medical sciences, ilam, iran elahe ranaei department of anatomy, faculty of medicine, ilam university of medical sciences, ilam, iran

introduction: congenital anomalies are a common cause of disability and mortality in newborns and their treatments involves high costs for the society. this study aimed to investigate the prevalence of congenital anomalies and their causes. materials and methods: this research was a descriptive-analytical study and the population included all the newborns in hospitals of the city of ilam in 201...

Journal: :iranian red crescent medical journal 0
a matic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected]; neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] s pricic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] m matic clinical centre of vojvodina, dermatovenereological clinic, serbia g velisavljev filipovic neonatology department, institute for child and youth health care of vojvodina, serbia 381216612172, [email protected] a ristivojevic neonatology department, gynaecologic-obstetric clinic, clinical centre of vojvodina, serbia

background cutis marmorata telangiectatica congenita (cmtc) is a sporadic congenital skin vascular abnormality. significant number of patients has other congenital anomalies. case report we report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. besides, microretrognatia and asymm...

Journal: :international journal of epidemiology research 0
leila rostamizadeh clinical biochemistry and laboratory sciences dept., division of medical genetics tabriz university of medical sciences, tabriz, i.r. iran sayed rafi bahavarnia tabriz blood transfusion organization, tabriz, i.r. iran roya gholami shahid-madani hospital, tabriz university of medical sciences, azarshahr, i.r. iran

background and aims: congenital anomalies are as the major causes of stillbirths, neonatal death, disability and childhood health problems all over the world. the aim of this study was to determine the incidence and pattern of congenital anomalies in newborn during the first 24 hours of life in shahid-madani hospital, azarshahr, tabriz, during two periods 2002-2003 and 2012-2013 years. methods:...

 جواد احمدی, ,  عبدالرزاق کیانی, ,  علیرضا ابراهیم سلطانی, ,  فرزانه کاظمیان, ,  مهرداد حسین پور, , فاطمه خاتمی, , منصور ملائیان, , مهرداد گودرزی, , هدایت‌اله نحوی, , ژامک خورگامی, ,

Background: Oral clefts are among the most common congenital anomalies. Infants with oral clefts often have other associated congenital defects, especially congenital heart defects. The reported incidences and the types of associated malformations and congenital heart defects vary between different studies. The purpose of this study was to assess the incidence of associated congenital heart def...

Journal: :iranian red crescent medical journal 0
shahla afsharpaiman health research center, baqiatallah university of medical sciences, tehran, ir iran mohammad saeid rezaee zavareh students’ research committee, baqiatallah university of medical sciences, tehran, ir iran; pediatric department, faculty of medicine, baqiyatallah university of medical sciences, tehran, ir iran; students’ research committee, baqiatallah university of medical sciences, tehran, ir iran. tel/fax: +98-2181264354 mohammad torkaman pediatric department, faculty of medicine, baqiyatallah university of medical sciences, tehran, ir iran

conclusions octreotide therapy as one of the conservative managements for cc can be considered before surgical methods. this treatment method also had some effects on the feeding initiation time and helped us to start feeding sooner. however, more studies like clinical trials are still necessary to investigate all aspects of octreotide treatment to determine the amount of its dose, initiation t...

Journal: :international journal of endocrinology and metabolism 0
mohammad reza alaei department of pediatric endocrinology, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iran susan akbaroghli genetic counseling division, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iran; mofid children’s hospital, tehran, ir iran. tel: +98-2122227033, fax: +98-2122227033 mohammad keramatipour department of medical genetics, school of medicine, tehran university of medical sciences, tehran, ir iran ali alaei school of medicine, shahid beheshti university of medical sciences, tehran, ir iran

conclusions congenital hyperinsulinism can have different inheritance pattern. autosomal recessive inheritance is more common but less frequently autosomal dominant inheritance can be seen. it appears that mutations in abcc8 gene can show both autosomal recessive and autosomal dominant inheritance of the disease. pcr followed by sanger sequencing proved to be an efficient method for mutation de...

Journal: :بینا 0
آزاده دوزنده a doozandeh shahid beheshti university of medical sciencesدانشگاه علوم پزشکی شهید بهشتی محمدرضا جعفری نسب mr jafarinasab shahid beheshti university of medical sciencesدانشگاه علوم پزشکی شهید بهشتی بهاره بهداد b behdad shahid beheshti university of medical sciencesدانشگاه علوم پزشکی شهید بهشتی محمدعلی جوادی ma javadi shahid beheshti university of medical sciencesمرکز تحقیقات چشم- دانشگاه علوم پزشکی شهید بهشتی سپهر فیضی s feizi shahid beheshti university of medical sciencesدانشگاه علوم پزشکی شهید بهشتی مهدی یاسری m yaseri دانشکده بهداشت و آمار- دانشگاه علوم پزشکی تهران محمدمهدی صدوقی

purpose: to report the refractive changes after intraocular lens (iol) implantation in children with congenital and developmental cataract. methods: in this historical cohort study, the clinical records of children between 2 and 15 years old that had lensectomy with posterior capsulotomy, anterior vitrectomy and iol implantation with more than 5 years of follow-up were studied. refractive error...

Journal: :iranian rehabilitation journal 0
younes lotfi university of social welfare and rehabilitation sciences, tehran, iran. gita movallali university of social welfare and rehabilitation sciences, tehran, iran.

objectives: in september 2002 university of social welfare & rehabilitation sciences established a pilot universal newborn hearing screening program in two crowded maternity hospital in tehran. our objective was to assess the feasibility of implementing universal newborn hearing screening in iran. methods: between september 2002 and march 2004 a total of 7718 newborns were screened for hearing ...

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