A boy with chest deformity
نویسندگان
چکیده
منابع مشابه
A boy with chest deformity.
An 11 year old boy with a right hemithorax deformity and diminished breathing sounds in the right lung was referred to our department, following examination by a physician due to knee pain caused by flat-footedness. He had a history of recurrent viral infections of the upper airways in early childhood since the age of 3 yrs. He has been free of pulmonary complaints. Bronchitis was diagnosed onl...
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Introduction: With respect to high association of skeletal chest deformity with cardiac abnormalities, these patients should be evaluated for evidence of cardiac involvement. So, we used echocardiography to investigate this association. Methods: This case-control study was done on 144 patients with skeletal chest deformity referred to OPD clinic. 240 persons were selected as control group, with...
متن کاملChest deformity, residual airways obstruction and hyperinflation, and growth in children with asthma. II. Significance of chronic chest deformity.
Gillam, G. L., McNicol, K. N., and Williams, H. E. (1970). Archives of Disease in Childhood, 45, 789. Chest deformity, residual airways obstruction and hyperinflation, and growth in children with asthma. Part II: Significance of chronic chest deformity. Studies were made on 56 10-11-year-old asthmatic children with onset of symptoms before 3 years of age, frequent and persistent attacks, and ob...
متن کاملproptosis, micrognathia, low set ear and chest deformity in a patient with extra marker chromosome 22
there is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma. the result of karyotype showed 47xx, with extra marker chromosome 22. although such a manifestation had not been reported in the literature, it should be considered as a very rare manifestati...
متن کاملProptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22.
There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma. The result of karyotype showed 47XX, with extra marker chromosome 22. Although such a manifestation had not been reported in the literature, it should be considered as a very rare manifestati...
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ژورنال
عنوان ژورنال: European Respiratory Journal
سال: 1996
ISSN: 0000-0000,0903-1936
DOI: 10.1183/09031936.96.09091962