Text Box: Newsletter
Otorhinolaryngology News
Abreast Of  Ear, Nose & Throat / Head & Neck Advances
30 December,  2005
Hello, All. Merry XMAS in arrears and HAPPY 2006 IN ADVANCE. You are Welcome to this week's ORL Update. I do hope you find my picks for this week exciting and useful
Biodun Olusesi, Newsletter Editor
ANOXIA and Cortical Language Processing.......

In an attempt to explain the neural basis for poor auditory and cortical language processing observed in disabled persons - Autism, language-impaired,  Schizophrenics, etc. Strata et al in an animal experiment (PNAS | December 27, 2005 | vol. 102 | no. 52 | 19156-19161) provided brief perinatal anoxia (PA) in rats and demonstrated that PA rats had increased acoustic thresholds and reduced processing efficiencies recorded in an auditory behavioral task

Abstract: Little is known about the neural bases of the reduced auditory and cortical processing speeds that have been recorded in language-impaired, autistic, schizophrenic, and other disabled human populations. Although there is strong evidence for genetic contributions to etiologies, epigenetic factors such as perinatal anoxia (PA) have been argued to be contributors, or causal, in a significant proportion of cases. In this article, we explored the consequences of PA on this elementary aspect of auditory behavior and on auditory system function in rats that were briefly perinatally anoxic. PA rats had increased acoustic thresholds and reduced processing efficiencies recorded in an auditory behavioral task. These rats had modestly increased interpeak intervals in their auditory brainstem responses, and substantially longer latencies in poststimulus time histogram responses recorded in the primary auditory cortex. The latter were associated with degraded primary auditory cortex receptive fields and a disrupted tonotopy. These processing deficits are consistent with the parallel behavioral and physiological deficits recorded in children and adults with a history of language-learning impairment and autism.

TOP PICKS

Genetic basis for Meniere's Disease...?
A new Japanese study by Katsumi Doi et al (ORL 2005;67:289-293) has demonstrated that Meniere's Disease might actually be the result of single nucleotide polymorphism (NSP) involving the K+ channel genes - KCNE1 & KCNE2

Abstract: Although the bases for both the sporadic and inherited forms of Ménière's disease (MD) remain undefined, it is likely to be multifactorial, one of the factors being a genetic predisposition. Recently, genetic association studies on complex diseases have become very popular and most of them are case-control studies using single nucleotide polymorphisms (SNPs) as markers. Mutations/polymorphisms in KCNE potassium channel genes might play a causative role in MD, because KCNE potassium channels have been suggested to be present and active in transmembrane ion and water transports in the inner ear. In the present study, to identify MD susceptibility genes, we have conducted a genetic association study with optimized sampling, optimized phenotyping/genotyping, and a selection of KCNE genes as the candidate genes. The SNPs analyses identified 112G/A SNP in the KCNE1 gene and 198T/C SNP in the KCNE3 gene in 63 definite MD cases as well as 205 and 237 non-MD control subjects. For both KCNE1 and KCNE3 genes, a significant difference in frequency of each SNP was confirmed between MD cases and non-MD control subjects. The result indicates that 112G/A SNP in the KCNE1 gene and 198T/C SNP in the KCNE3 gene could determine an increased susceptibility to develop MD.


Coming Events of Importance to Otolaryngologists in Africa...
 

  1. Annual West Africa College of Surgeons Conference, Accra, Ghana, Feb 2006.
  2. Association of Paediatric Otolaryngologists of India 12th Annual Conference and CME in Paediatric Otolaryngology
    February 25-26, 2006; New Delhi, India
  3. 8th International Otology Course of the Jean Causse Ear Clinic
    June 22-24, 2006; Béziers, France
  4. 110th American Academy of ORL,Head & Neck Surgery Annual Meeting & OTO EXPO
    September 17-20, 2006;
    Toronto, Canada.
  5. 42nd South African ENT Congress joint meeting with the British Association of Otolaryngology - Head & Neck Surgery
    October 29-November 1, 2006;
    Cape Town, South Africa.

         For more courses and workshops and conferences....Click Here


Auditory-Visual Fusion in Young Cochlear Implantees.....?       

Schorr, Fox, van Wassenhove & Knudsen in a recent paper  (PNAS | December 20, 2005 | vol. 102 | no. 51) demonstrated that majority of children with cochlear implants, when presented with conflicting auditory and visual stimuli rely more on vision, while some of these children maintain consistent bimodal auditory-visual fusion.

Text Box: Previous Newsletter
Abstract: Speech, for most of us, is a bimodal percept whenever we both hear the voice and see the lip movements of a speaker. Children who are born deaf never have this bimodal experience. We tested children who had been deaf from birth and who subsequently received cochlear implants for their ability to fuse the auditory information provided by their implants with visual information about lip movements for speech perception. For most of the children with implants (92%), perception was dominated by vision when visual and auditory speech information conflicted. For some, bimodal fusion was strong and consistent, demonstrating a remarkable plasticity in their ability to form auditory-visual associations despite the atypical stimulation provided by implants. The likelihood of consistent auditory-visual fusion declined with age at implant beyond 2.5 years, suggesting a sensitive period for bimodal integration in speech perception.

 

Case Review
 
CLINICAL RADIOGRAPH OF THE WEEK

A 30-year old female was referred from the neurology clinic where she had presented with insomnia of 3 months duration following a near-fatal accident involving a car she was travelling in. She sustained no injury during the near-fatal accident. Examination was essentially normal. MRI brain revealed the feature (red arrow) on this picture. You way want to see the axial view of contrast-enhanced MRI

What is the diagnosis?

Parting Shot...
If you have an interesting case to discuss or share with other Otolaryngologists all over Africa, feel free to email Me or at best go to otolaryngology in Africa blogsite and post your case

Also, if you are among those who requested for a copy of DODA at the last ORLSON Meeting @ Port Harcourt, please take time to view the DODA - FAQ page, and expect your copy of the program soon. The current delay is due to adding more features to the DODA program as well as pruning some features you might really not need for initial assessments

Expect a newer and more richer Newsletter in 2006.

Till Next Year,

Biodun

 

 

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© Copyright Dr 'Biodun Olusesi,  2005

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