منابع مشابه
congenital brucellosis in an infant
background brucellosis is a zoonotic disease involving several organs with different presentations. it is primarily a disease of animals. human infection is usually acquired by close contact with infected animals or consumption of unpasteurized dairy products. the major reservoirs include goat, sheep, swine and cattle. human to human transmission of brucellosis is a rare entity, especially peri...
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Total or partial fissure in the middle of the sternum (cleft sternum or fissura sterni congenita) is a rare congenital anomaly. Absence of skeleton in the front part of the chest wall gives rise to a severely paradoxical movement of this part of the thorax (Figs 1 and 2). Moreover, the pulsations of the heart and large vessels are clearly visible because they are covered only by soft tissues. T...
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We are reporting an infant with persistent abnormal liver function, neonatal jaundice, and intermittent hypoglycemia. Evaluation confirmed congenital hypopituitarism, in the absence of congenital anomalies and midline defect. His jaundice and abnormal liver function improved after treatment with Levothyroxine and hydrocortisone.
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Congenital absence of left circumflex artery is a rare congenital anomaly of the coronary arteries. The prevalence of the anomaly in different studies ranges from 0.6% to 1.3%. Of these, 80% are benign and asymptomatic and 20% are clinically important. We report a 56-year-old man presented with acute resting chest pain who was diagnosed as having acute anterolateral infarction accompanied by el...
متن کاملCFTR Mutations in Congenital Absence of Vas Deferens
A qualitative diagnosis of infertility requires attention to female and male physical abnormalities, endocrine anomalies and genetic conditions that interfere with reproduction. Many genes are likely to be involved in the complex process of reproduction. Cystic fibrosis (CF) incidence varies in different White people populations (a higher incidence of CF is observed in northern–western European...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2017
ISSN: 1757-790X
DOI: 10.1136/bcr-2016-219081