نتایج جستجو برای: congenital anomalies

تعداد نتایج: 152444  

ژورنال: پوست و زیبایی 2019
Ayatollahi, Azin , Variji, Zeinab ,

Introduction: Beckers’s nevus is a cutaneous hamartoma which usually appears as a circumscribed hyperpigmentation with hypertrichosis. It usually presents unilaterally and the usual site is shoulder and scapula. It is rarely congenital and it is usually noticed first during adolescence. Case Report: Herein, we report a congenital bilateral large Becker’s nevus with positive familial history ...

Journal: :Archives of disease in childhood 2002
S Dastgiri D H Stone C Le-Ha W H Gilmour

AIM To describe the epidemiology of congenital anomalies in Glasgow with special reference to secular trends. METHODS The prevalence of congenital anomalies was determined retrospectively in 233 777 births using the Glasgow Register of Congenital Anomalies for the period 1980-97. RESULTS The total prevalence of congenital anomalies was 324 per 10 000 births, declining by just over a third f...

Introduction: Intraoral synechia is a rare congenital condition, generally associated with other maxillo-facial malformations. We present a neonate with congenital intraoral bilateral synechia without any other facial anomalies.   Case Report: In this paper, we present a 19-day-old male neonate with congenital intraoral bilateral synechia without any other facial anomalies. We review the litera...

2012
Emilio Antonio Luca Gianicolo Antonella Bruni Enrico Rosati Saverio Sabina Roberto Guarino Gabriella Padolecchia Carlo Leo Maria Angela Vigotti Maria Grazia Andreassi Giuseppe Latini

BACKGROUND Congenital anomalies and their primary prevention are a crucial public health issue. This work aimed to estimate the prevalence of congenital anomalies in Brindisi, a city in southeastern Italy at high risk of environmental crisis. METHODS This research concerned newborns up to 28 days of age, born between 2001 and 2010 to mothers resident in Brindisi and discharged with a diagnosi...

2015
James Ker

Congenital anomaly of the inferior vena cava (IVC) is a well described phenomenon [1,2]. These anomalies include complete absence, partial absence or duplication of the IVC [3]. Such anomalies of the IVC are seen more frequently in those with other congenital cardiac anomalies (0.6%–2%) [4]. This congenital condition can be discovered incidentally, or due to symptoms of associated congenital he...

Journal: :Archives of disease in childhood. Fetal and neonatal edition 2007
Peter O D Pharoah

BACKGROUND It has been hypothesised that cerebral palsy (CP) and other congenital anomalies are attributable to feto-fetal transfusion problems in a monochorionic multiple gestation. Thus more than one organ could be compromised leading to the coexistence of two or more anomalies in a fetus. Such anomalies in a singleton birth may be attributable to early demise of the co-conceptus as a vanishi...

2011
Maria Arafah Deena T. Boqari Khaled O. Alsaad

Congenital diaphragmatic hernia is a common congenital anomaly of uncertain etiology. Its association with multiple congenital anomalies in various organs is well recognized and antenatal radiological evidence of congenital diaphragmatic hernia warrants thorough evaluation to detect other anomalies, some of which can be life threatening. Rarely, heterotopic hepatic tissue is identified in the h...

 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: :The Journal of pediatrics 2009
Juhi Kumar Roberto Gordillo Frederick J Kaskel Charlotte M Druschel Robert P Woroniecki

OBJECTIVE We investigated the prevalence of congenital renal and urologic anomalies in children with congenital hypothyroidism to determine whether further renal and urologic investigations would be of benefit. STUDY DESIGN Prevalence of congenital hypothyroidism was obtained from the New York State Congenital Malformation Registry. The occurrence of urinary tract anomalies were calculated fo...

Journal: :Saishin igaku. Modern medicine 1967
H Nishimura

85 Epigenetic abnormality of SRY gene in the adult XY female with pericentric inversion of the Y chromosome Tomoko Mitsuhashi, Katsuhiko Warita, Teruo Sugawara, Yoshiaki Tabuchi, Ichiro Takasaki, Takashi Kondo, Fumio Hayashi, Zhi-Yu Wang, Yoshiki Matsumoto, Takanori Miki, Yoshiki Takeuchi, Yasuhiko Ebina, Hideto Yamada, Noriaki Sakuragi, Toshifumi Yokoyama, Takashi Nanmori, Hiroshi Kitagawa, Je...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید