Bilateral Pulmonary Agenesis

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Bilateral pulmonary agenesis, oesophageal atresia, and the first arch syndrome.

Absence of both lungs is extremely rare; there appear to be only four recorded cases (Claireaux and Ferreira, 1958 ; Tuynman and Gardner, 1952; Allan and Affelbach, 1925 ; Schmit, 1893). Oesophageal atresia has a frequency of about 1: 3,500 births and the first arch syndrome is uncommon. The occurrence of all three of these conditions in a liveborn infant has not previously been recorded and it...

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Prenatal Diagnosis of Bilateral Pulmonary Agenesis: a Case Report

We report a case of bilateral pulmonary agenesis (BPA), which was suspected during a prenatal US examination and diagnosed by fetal magnetic resonance imaging (MRI). BPA is an extremely rare congenital anomaly and, although many fetal structural defects can be detected with a high degree of confidence after introducing high-resolution US, the prenatal diagnosis of BPA remains problematic. Other...

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Pulmonary agenesis.

B. Rajshekhar Case Reports Sunil Gomber Anurag Krishna* Five cases of pulmonary agenesis diag nosed at G.T.B. Hospital, Delhi are present ed. Four cases presented with recurrent history of chest infection and respiratory Pulmonary agenesis is an extremely distress for the last 1 months to 2 years. All rare condition with a reported prevalence these patients were being treated by priof 34 per 10...

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Pulmonary Agenesis.

Unilateral opaque lung with ipsilateral mediastinal shift is an uncommon cause of respiratory distress in newborn which can be found on simple radiograph of the chest. Pulmonary agenesis is a rare cause of unilateral opaque lung in the newborn. Nearly 50% cases of pulmonary agenesis are associated with other congenital defects including cardiovascular, skeletal, gastrointestinal or genitourinar...

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Pulmonary Artery Agenesis with Bronchial Asthma

Unilateral Pulmonary Artery Agenesis (UPAA) is a rare congenital anomaly during the 4 th  week of gestational age. It is defined as an absence of pulmonary parenchyma and its supporting artery. A 9-year-old girl was admitted to our hospital because of chronic cough. Chest examination showed a decrement in lung sound of right hemi-thorax with expiratory wheeze. Chest radiography (CXR) revealed a...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1958

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.33.170.364