نتایج جستجو برای: congenital

تعداد نتایج: 120294  

Background: Goiter is not frequently seen in the neonatal period.Case report: We report the case of a full-term neonate who was born with anterior neck swelling and observed tosuffer from congenital goiter on examination. Thyroid function tests were within normal limits. Thyroid swellinggradually reduced in size during the 1st week of life. All the cases of congenital goiter t...

Journal: :acta medica iranica 0
z moinfar f. davari tanha z. moinfar m. kaveh s. eftekhari s. eftekhari z. khalilpour

short rib polydactyly syndrome (srps) is a very rare congenital anomaly that is classified into four subtypes. it is an autosomal recessive inherited disease. we report a case of this syndrome without a previous family history of congenital defects.

Saadollah Shamsaldini,

Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic defor...

Amiri , F, Ghorbani , E, Mirrashidi, FS, Mirzaee, M, Nasiri, N, Sharifi, H,

Background and Objectives: Congenital hypothyroidism is one of the reasons for mental retardation and premature death of infants. Since identification of the determinants of hypothyroidism plays a significant role in its prevention, this study was conducted to determine the prevalence of congenital hypothyroidism and to investigate its determinants in newborn infants.   Methods: This study wa...

ژورنال: طب جنوب 2020
Dalili , Satila, Gholi Famian , Ali Reza, Hassanzadeh Rad , Afagh, Rovshan , Belghes,

Background: Congenital hypothyroidism is one of the most common endocrinology diseases in children. Given the importance of evaluating the normal growth and development and identifying growth and development abnormalities, this study aimed to evaluate the developmental skills of patients with congenital hypothyroidism and healthy children. Materials and Methods: This controlled cross-sectional...

2013
Mirjana A. Janicijevic-Petrovic Tatjana S. Sarenac-Vulovic Katarina M. Janicijevic Dragan I. Vujic Dejan D. Vulovic

CONFLICT OF INTEREST none declared. INTRODUCTION Authors are from reference documentation to archive at Organization of Federation of blind and visually impaired in central Serbia (Kragujevac), by retrograde analysis, of 2007-2012, comprehend two groups by etiology-clinical characteristics of congenital blindness and visually impaired, caused infection or non infection example. AIM to analy...

Journal: :the journal of tehran university heart center 0
maryam moradian rajaie cardiovascular medical and research center, tehran university of medical sciences, tehran, ir

echocardiography is considered the primary diagnostic tool for congenital heart diseases. the pediatric echocardiography diagnostic errors, consisting of false positive or discrepant diagnoses, picked up within a 2.5-year period in our pediatric echocardiography laboratory are presented herein. in this case report, the factors contributing to the diagnostic errors are categorized as cognitive s...

Journal: :the journal of tehran university heart center 0
kiyomars abbasi tehran heart center, tehran university of medical sciences, tehran, iran. hakimeh sadeghian tehran heart center, tehran university of medical sciences, tehran, iran. neda ghafari-marandi tehran heart center, tehran university of medical sciences, tehran, iran. afsaneh sadeghian fatemieh hospital, shahrood university of medical sciences, shahrood, iran.

cor triatriatum is defined as a membrane within the left atrium, which might lead to restricted pulmonary venous return. diagnosis is usually achieved by echocardiography in early infancy. therapy of choice is the excision of the membrane. herein, successful correction of cor triatriatum in a 4-year-old girl is presented, and the clinical features, echocardiographic findings, and the surgical t...

Journal: :مجله دانشکده پزشکی اصفهان 0
احمد میردامادی استادیار، گروه قلب، دانشکده ی پزشکی، دانشگاه آزاد اسلامی، واحد نجف آباد، اصفهان، ایران سمیرا اشرفی کارشناس ارشد، آزمایشگاه تحقیقاتی، دانشگاه اصفهان، اصفهان، ایران

pulmonary arterial hypertension (pha) is a frequent complication of congenital heart disease (chd), most commonly in systemic-to-pulmonary shunt lesions. in patients with an uncorrected left-to right shunt, pah will end up to eisenmenger’s syndrome, which is contraindication of surgery. what about patients with moderate to severe pah, who do not have criteria of eisenmenger’s syndrome; immediat...

Journal: :iranian journal of public health 0
ia rad dept. of genetics, motahhari hospital, urmia university of medical sciences, iran ar afshar dept. of orthopedics, imam hospital, urmia university of medical sciences, iran

maternal hyperglycemia during early gestation is associated with an increased incidence of congenital anomalies. a case of mater­nal diabetes syndrome is presented here with a rare constellation of congenital anomalies, i.e., bifurcated distal pha­lanx of the thumb, patent ductus arteriosus and cleft lip.

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