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Otorhinological disorders among pregnant women attending the obstetric clinic at Benjamin Mkapa Hospital, Tanzania.
Niger Med J
January 2025
Department of Otorhinolaryngology, Muhimbili University of Health and Allied Sciences, Dares Salaam, Tanzania.
Background: Pregnancy leads to physiological changes primarily driven by hormones like oestrogen and progesterone. Such changes are multi-systemic in nature including involvement of the ear, nose and throat. Such changes impair the quality of the life of pregnant women and thus requires prompt intervention during pregnancy.
View Article and Find Full Text PDFSpectrum of Otological Manifestations in Treacher Collins Syndrome: A Case Series of 9 Patients.
J Comput Assist Tomogr
January 2025
Department of Diagnostic Radiology and Nuclear Medicine, Rush University Medical Center, Chicago, IL.
Treacher Collins syndrome (TCS) is an uncommon congenital disorder predominantly involving craniofacial, orbital, and otological structures. The various ear malformations seen in 9 patients with TCS are described. TCS predominantly affects the external and middle ear structures, with inner ear structures being relatively spared, not unexpected given the dual embryological origin of the human ear.
View Article and Find Full Text PDFComprehensive Clinical and Genetic Characterization of Kabuki Syndrome: A Case Series Study.
J Child Neurol
December 2024
Department of Clinical and Experimental Medicine, University Hospital "Policlinico-San Marco of Catania, Catania, Italy.
Kabuki syndrome is a rare congenital disorder characterized by a distinctive combination of craniofacial features, developmental anomalies, and intellectual disabilities. This study aims to provide a comprehensive exploration of Kabuki syndrome through a meticulous case series analysis focusing on its clinical features and genetic underpinnings. A cohort of 9 Kabuki syndrome patients was identified through a retrospective examination of medical records spanning from 1996 to 2022.
View Article and Find Full Text PDFOtologic Manifestations in Patients with Achondroplasia: A Multicenter Study.
J Int Adv Otol
November 2024
Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea.
Background: Achondroplasia, the most prevalent form of skeletal dysplasia involving short stature, necessitates a multidisciplinary approach that includes otology and auditory rehabilitation. Despite this, the clinical characteristics of hearing loss and otologic manifestations in achondroplasia patients remain poorly defined. This study aimed to explore the prevalence and treatment outcomes of otologic disease in individuals with achondroplasia.
View Article and Find Full Text PDFFirst Branchial Cleft Anomaly Mimicking Cholesteatoma: A Pediatric Case Study and Surgical Approach.
Am J Case Rep
November 2024
Department of Otorhinolaryngology-Head and Neck Surgery, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Article Synopsis
- First branchial cleft anomalies (FBCAs) are rare congenital disorders that can cause variable symptoms and complex anatomical issues, often misdiagnosed as other conditions like cholesteatoma.
- A 4-year-old girl presented with a painless mass in her left ear, leading to a thorough diagnostic process involving multiple imaging techniques that confirmed an FBCA.
- Surgical intervention to resect the fistula was successful, with no postoperative complications or recurrence, emphasizing the need for precise diagnosis and treatment in such cases.
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