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BACO: The Master’s role
Ian Mackay is this year’s BACO Master, with Valerie Lund taking over for the next meeting. As the senior overseer of the conference, the role of Master is a crucial one, and Ian tells us how he has gone about...
Endoscopic Ear Surgery: Principles, Indications and Techniques
I was delighted to be asked to review this book. It’s big and shiny, and has 400 pages, many of which bear beautiful colour images including endoscopic photographs, radiological images and clear illustrations of middle ear anatomy. The preface to...Genetic foundations of Ménière’s disease: changing the game
Sydney researchers reveal genetic roots of Ménière’s disease. Familial patterns and gene discoveries highlight autosomal inheritance in rare cases, transforming molecular insights. Ménière’s disease (MD) is a chronic disorder of the inner ear defined by clinical criteria of episodic vertigo...
Atlas of Otologic Surgery and Magic Otology, Second Edition
After having read a variety of books that focus on otology, the Atlas of Otologic Surgery and Magic Otology provides a complete and holistic perspective on the field of otology, including a wide range of topics such as structure and...
MRI and the endolymphatic space
This is an interesting study which was performed to evaluate the endolymphatic space in patients with endolymphatic hydrops (EH), using MR imaging. Seven patients aged between 21–77 years; five female, two male with unilateral or bilateral symptoms of EH were...
Mondini dysplasia and cochlear implantation
Approximately 20-28% of sensorineural hearing loss in children arises due to a cochlear malformation. Mondini dysplasia includes a cochlear with one and a half turns and an incomplete interscalar septum. Cochlear implantation is a common treatment protocol for children with...
Genetics of IP-III
The authors provide a literature review of the genetic basis and clinical features of incomplete partition (IP)-type III. The condition is seen typically in males and is due to mutation in the POU class 3 homeobox 4 (POU3F4) gene which...
