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Toplam kayıt 66, listelenen: 61-66
Polyposis Deserves a Perfect Physical Examination for Final Diagnosis: Bannayan-Riley-Ruvalcaba Syndrome
(Turkish J Pediatrics, 2017)
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal dominant inherited polyposis syndrome characterized by macrocephaly, lipomatosis, hemangiomatosis, intestinal polyposis and pigmented macules on penis. The ...
Persistent Eyelid Swelling in a Child: Lest Myiasis Be Forgot
(Springer, 2014)
Myiasis involving the eyelid is uncommon. Herein, we present an 8-year-old boy who was diagnosed with preseptal cellulitis, yet a single larva was eventually extracted from his eyelid.
An International Consortium Update: Pathophysiology, Diagnosis, and Treatment of Polycystic Ovarian Syndrome in Adolescence
(Karger, 2017)
This paper represents an international collaboration of paediatric endocrine and other societies (listed in the Appendix) under the International Consortium of Paediatric Endocrinology (ICPE) aiming to improve worldwide ...
Prevalence and Seasonal Distribution of Viral Etiology of Respiratory Tract Infections in Inpatients and Outpatients of the Pediatric Population: 10 Year Follow-Up
(Turkish J Pediatrics, 2018)
The aim of this study was to investigate the prevalence and seasonal distribution of respiratory viruses in pediatric patients. Nasopharyngeal swab specimens, demographic and clinical information were collected from 1240 ...
Vasculitis: Do We Know More To Classify Better?
(Springer, 2015)
The systemic vasculitides are a heterogeneous group of disorders characterized by the inflammation of blood vessels. The development and implementation of advanced diagnostic tests and genetic studies have resulted in ...
A Novel De Novo Mutation Involving the Mll2 Gene in a Kabuki Syndrome Patient Presenting with Seizures
(Turkish J Pediatrics, 2016)
Kabuki syndrome is a rare multiple congenital anomaly disorder. Although mental retardation is one of the main features, various neurological symptoms such as hypotonia and seizures can occur. Here we report on a 18-year-old ...