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Otorhinolaryngology News
Abreast Of Ear, Nose &
Throat / Head & Neck Advances
30 December, 2005
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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 |
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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.
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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...
- Annual West Africa
College of Surgeons Conference, Accra, Ghana, Feb
2006.
-
Association of Paediatric Otolaryngologists of
India 12th Annual Conference and CME in Paediatric
Otolaryngology
February 25-26, 2006; New Delhi, India
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8th International Otology Course of the Jean Causse
Ear Clinic
June 22-24, 2006; Béziers, France
-
110th American Academy of ORL,Head & Neck Surgery
Annual Meeting & OTO EXPO
September 17-20, 2006;
Toronto, Canada.
-
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.
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.
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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
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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 |