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Nasal dermal sinus cysts with intracranial extension in a child mosaic for a supernumerary ring chromosome 20
27 January 2012
Bernarda Lozić, Draško Cikojević, Vlatko Ledenko, Marisa Klančnik, Ružica Lasan, Tatijana Zemunik
Abstract: Nasal dermal sinus cysts are congenital malformations that result from anomalous embryological development and are not prescribed to any specific genetic defect. The occurrence of a supernum...
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Subglottic stenosis in juvenile rheumatoid arthritis
19 January 2012
Chafeek Tomeh, Nicholas Jones, Parker Velargo, Jerome Thompson
Abstract: Juvenile rheumatoid arthritis (JRA), now termed juvenile idiopathic arthritis (JIA), is a well-described group of arthritides in the pediatric population with known associations with airway ...
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Esophageal squamous cell carcinoma in children: A case presentation and review of an unusual entity
09 January 2012
Nilda Süslü, Rezarta Taga Senirli, A. Şefik Hoşal, Burce Özgen Mocan, Mustafa Cengiz
Abstract: Squamous cell carcinoma (SCC) of the esophagus usually occurs between the 4th and 6th decades of life. Esophageal SCC in children is an extremely rare entity – only a few pediatric and adole...
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Postextubation stridor in a child with asymptomatic trifid epiglottis with polydactyly – A rare case report
06 January 2012
Sameer Sethi, K.S. Vadaje, Ashok K. Gupta
Abstract: Trifid epiglottis is an extremely rare congenital laryngeal anomaly. Trifid anomaly of epiglottis has not been described in literature. In the embryo, epiglottis, hypothalamus, and digital b...
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Wegener's granulomatosis with bilateral facial nerve paresis and bilateral profound sensorineural hearing loss
16 December 2011
Raman Wadhera, Sat Paul Gulati, Vijay Kalra, Anju Ghai
Abstract: Wegener's granulomatosis (WG) is a fatal disease. Facial nerve paralysis in association with WG is rare, being present in about 5% of patients, alone or in combination with hearing loss and ...
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