Pneumoperitoneum in a patient with Larsen syndrome
نویسندگان
چکیده
منابع مشابه
Dextrocardia and Hiatal Hernia in a Patient with Turner Syndrome
Turner syndrome is a sex-chromosome disorder occurring in one out of 2500 female births and characterized by growth retardation, gonadal dysgenesis and cardiovascular anomalies. The 45, XO karyotype is the most frequent type of this disease. Herein, we report on a 6-year-old girl with Turner syndrome and 45, XO karyotype presenting with short stature. She had dextrocardia and hiatal hernia. To ...
متن کاملSinding-Larsen-Johansson syndrome
History and clinical findings A 12-year-old boy presented to a paediatric rheumatology clinic with a 2-month history of painful knees. He had been referred from the paediatric oncology department with a previous diagnosis of acute lymphocytic leukaemia, in remission for 5 years. The pain was felt just below the patella, especially after a game of soccer, climbing stairs or walking for long dist...
متن کاملTreating a Patient with Bone Marrow Edema Syndrome with Iloprost
Bone Marrow Edema Syndrome (BMES) is an uncommon, self-limited and with unknown etiology characterized by severe pain with no history of trauma. Due to low prevalence of BMES and its non-specific signs, correct diagnosis is often delayed intensifying bone pain and impairing patients’ function and quality of life. In this study we treated a patient with bone marrow edema syndrome in right a...
متن کاملImage of pneumoperitoneum in patient with phytobezoar.
A 61 year-old-man was referred to the emergency room with intense and acute epigastric pain after a large meal, without experiencing symptoms of nausea or vomiting. His medical history included obsessive neurosis and a Billroth I gastric resection due to a duodenal ulcer. The patient was hemodynamically stable and had a distended abdomen that was painful to the touch, with maintained peristalsi...
متن کاملa large multigeneration iranian family with autosomal dominant larsen syndrome
larsen syndrome is a skeletal dysplasia (osteochondro-dysplasia) in which multiple dislocations of the large joints are the major feature . nosology in this group of disease, which constitutes 8% of mendelian disorders in man, is primarily based on clinical and radiological features. the underlying genetic defect is 3p21.1-p14.1 in the dominant type
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ژورنال
عنوان ژورنال: Journal of Anesthesia
سال: 2013
ISSN: 0913-8668,1438-8359
DOI: 10.1007/s00540-013-1742-1