Kartagener's Syndrome with Fibrocystic Disease
نویسندگان
چکیده
منابع مشابه
Spinal anesthesia in Kartageners syndrome.
Kartageners syndrome, an autosomal recessive disorder is a combination of dextrocardia situs inversus, bronchiectasis and sinusitis. We report a 22-year-old woman with this syndrome scheduled for appendectomy. Spinal anesthesia was preferred for the patient with this rare disorder due to the relative advantages of the regional technique over general anesthesia.
متن کاملFibrocystic disease of the pancreas presenting with acute salt depletion.
During the hot summer of 1948, 10 patients were admitted to the Babies' 1Ipspital in New York with heat prostration. No fewer than five of these children were cases of fibrocystic disease of the pancreas. Two further cases were discovered in subsequent summers. Reporting this interesting observation, Kessler and Andersen (1951) recorded that this special susceptibility to heat occurred in child...
متن کاملElmslie and Fibrocystic Disease of Bone
The value of legislation and the speed with which it may be introduced depends to a large extent upon public opinion. In a special supplement on the Factory Act of 1937 an earlier statement of the Times on public health legislation is quoted 'Mr. Chadwick and Dr. Southwood Smith have been deposed. The people of England prefer to take their chance with cholera and the rest rather than be bullied...
متن کاملFibrocystic disease of the pancreas with meconium peritonitis at birth.
Case Report L.M., a male infant, was delivered spontaneously on August 21, 1949, at full term, after a normal pregnancy, and weighed 6 lb. 10 oz. Both parents and one sibling were normal and healthy. At birth the infant's abdomen was large and tense (girth 37 cm. at six hours) and a right hydrocoele was present. He showed a mild degree of asphyxia, but respirations were established satisfactori...
متن کاملIncidence of fibrocystic disease in Wessex.
Since the description of fibrocystic disease as a definite entity in 1936, many varied incidence figures have been published. The wide range in these figures has left doubt as to its true incidence. The present paper attempts to avoid previous sources of error, and the resultant values are expected to represent a reliable guide for future surveys. The condition is autosomal recessive, and until...
متن کاملذخیره 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: BMJ
سال: 1959
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.2.5154.725