Antenatal diagnosis of isolated omphalocele

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Antenatal diagnosis of isolated omphalocele

The concern of obstetric and surgical teams is when diagnosis of omphalocele, the care of the newborn and the prognosis of the malformation, mainly linked to the existence of associated malformations or chromosomal abnormalities. In our case of isolated omphalocele, the overall prognosis was good.

متن کامل

Diagnostic antenatal d’une omphalocele au premier trimester

We conducted a case study through the images of an omphalocele diagnosed in the first trimester of pregnancy in a Prenatal Diagnostic Unit in order to highlight the central role of early detection of foetal malformations. We here report the case of a 42year old G2P1 patient who underwent her first ultrasound at 12w + 4d of pregnancy showing an omphalocele (A,B,C,D). The patient was informed abo...

متن کامل

Antenatal diagnosis of achondroplasia

We report a interesting case of antenatal diagnosis of achondrpoplasia in a young multigravida who presented with term pregnancy for routine ultrasound assessment which revealed a single, live intrauterine fetus with a discrepancy between femur length (FL) and biparietal diameter (BPD), narrowing of the interpeduncular distance. The diagnosis of achondroplasia was made with a sonological skelet...

متن کامل

Outcome of isolated antenatal hydronephrosis.

OBJECTIVE To define the clinical outcome in isolated antenatal hydronephrosis (ANH), defined as pelviectasis without vesicoureteral reflux or urinary tract obstruction. STUDY DESIGN AND PATIENTS We analyzed prospectively gathered data from patients with isolated ANH. Pelviectasis, graded using the anterior-posterior diameter reference criteria, was defined by the status of the more severely a...

متن کامل

Antenatal diagnosis of seckel syndrome.

Evaluation of the fetus in a 29-year-old primigravida showed severe intrauterine growth restriction with complex brain malformation with fetal dysmorphology. The family and past obstetric history is unremarkable, with nonconsanguineous marriage. Her previous scans included one at 12 weeks for nuchal translucency, and another an anomaly scan at 19 weeks, which both were unremarkable. In late sec...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Pan African Medical Journal

سال: 2015

ISSN: 1937-8688

DOI: 10.11604/pamj.2015.21.233.7151