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Causapedia Türk Tıp dizininde....

Türk Tıp dizininde....

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Tıpta İyi Yazı Yazma Klavuzu

Dr. Hamdi Akan ve Dr. Bahadır Güllüoğlu'nun editörlüğünde e-Kitap olarak hazırlanan Tıpta İyi Yazı Yazma Kılavuzu internette http://www.tiptayazimkilavuzu.org adresinde yayına başlamıştır.

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Edwards Syndrome

Edwards syndrome (ES) is a syndrome with severe fatal anomalies resulting from malformations of the 18th chromosome seen in 8000 live births. The male / female ratio is 1/4. Ninety percent of newborn babies die in the first twelve months. Patients have moderate mental retardation, muscle hypotonia and extremity anomalies, microcephaly, facial anomalies, developmental disorders, scoliosis, epilepsy...

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Giant Fecaloma

Introduction: Fecaloma which is characterized by massive stony masses that are often localized in the sigmoid colon and rectum. Fecaloma can cause serious complications. Perforation of the gastrointestinal system may occur prolonged pressure of the fecal compartment, and progress of the obstruction. Case Report: A seventy-seven-year-old male patient was admitted to the emergency service due to ...

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Pelvic Mass

In female patients, pelvic masses are frequently originate from the reproductive organs. In addition, pelvic masses may arise from the gastrointestinal system, urinary system, neurogenic and soft tissues and metastases. In this paper, we present a 75-year-old female patient with a pelvic mass....

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Obturator Hernia

Obturator hernia is a rare variety of hernias. It originates from the obturator canal and has a high mortality rate. Especially in elderly patients with mechanical obstruction, it can be diagnosed quickly by computed tomography, so that emergency surgery can be performed. We report a case with obturator hernia in order to emphasize that the diagnosis and early intervention are the most import...

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Crouzon Syndrome with Multiple Anomalies

Crouzon syndrome, also known as craniofacial dysostosis, is an autosomal dominant congenital syndrome that affects the skull and facial bones. Genetic defect resulting from FGFR-2(fibroblast growth factor receptor 2) gene mutation is the clinical result. Craniosynostosis, maxillar hypoplasia, shallow orbit, ocular proptosis and hypertelorism are characteristic features of Crouzon syndrome. In this...

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