Gallbladder Duplication, Annular Pancreas and Duodenal Stenosis in a Child with Noonan Syndrome

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Gallbladder Duplication, Annular Pancreas and Duodenal Stenosis in a Child with Noonan Syndrome

Noonan syndrome occurs in about one per 2000 live births [1]. The males and females are affected equally. The disorder is usually sporadic, but presents also with dominant inheritance. The main features of Noonan syndrome are characteristic facial changes, such as: triangular face, hypertelorism, epicanthus, downward palpebral fissures, ptosis, micrognathia, low-set ears with thickened helices;...

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Gallbladder Duplication Associated with Duodenal Atresia

Gallbladder duplication is an extremely rare anomaly. Association of gall bladder agenesis with duodenal atresia and biliary atresia has been described. However, association of gall bladder duplication with duodenal atresia hasn't been described so far; we report a case in view of its rarity.

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Annular pancreas associated with duodenal obstruction.

DESCRIPTION A preterm neonate weighing 1360 g was born at 33+2 weeks’ gestation with severe polyhydramnios. She was transferred, directly after delivery, to our neonatal intensive care unit presenting with distended upper abdomen and vomiting. A plain film of the abdomen (figure 1) was performed with the suspicion of duodenal atresia and showed a markedly distended stomach (S) and proximal duod...

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Abnormal Auditory Brainstem Response (ABR) Findings in a Near-Normal Hearing Child with Noonan Syndrome

Introduction: Noonan syndrome (NS) is a heterogeneous genetic disease that affects many parts of the body. It was named after Dr. Jacqueline Anne Noonan, a paediatric cardiologist.Case Report: We report audiological tests and auditory brainstem response (ABR) findings in a 5-year old Malay boy with NS. Despite showing the marked signs of NS, the child could only produce a few meaningful words. ...

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Introducing a Specimen of Annular Pancreas (with late-onset Symptoms)

Annular pancreas is a relatively rare congenital diseasecaused by an embryologica1and anatomical disturbance in pancreas It may have no sympforns throughout the life and so occasionally discovered during an unrelevant surgery or autopsy but in most of the cases it shows itself as a duodenal obstruction during the in­fancy and childhood.Very rarely symptoms of the disease my be obser­ved in adul...

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ژورنال

عنوان ژورنال: Advanced Research in Gastroenterology & Hepatology

سال: 2017

ISSN: 2472-6400

DOI: 10.19080/argh.2017.06.555682