Text Box: January 23, 2007

Text Box: Otorhinolaryngology News

Text Box: Inside This Issue
· LigNext thing After Kemp.?
· ILS - Still Confusing..?
· TinCx26 SNHL - Cong. or Acquired.? 
*     Case of the Week

 

 

 Case Review

 Clinical Radiograph of The Week

A 6-year old male was brought by the mother following history of right ear pain of a month duration. He lives with an uncle in another town following inability of the mother to secure a job. Cross examination revealed he was occasionally maltreated by the guardian. Examination was negative except for the sign displayed on this picture

 

What is the Diagnosis

1.     25th Alexandria Combined ORL Congress, April 18 - 20 2007; Alexandria, Egypt. Deadline for Abstract submission January 15, 2007. Click HERE for Details

2. 

 

 

 

3.      IX éme Congrès Panafricane d'ORL et de Chirugie Cervicofaciaie (PAFOS)  & XXX éme Congrès National Société           Marocaine d'ORL. 2007. April 28 - 31. Abstracts before 15th January, 2007 email benghalem@wanadoopro.ma .         Hotel Booking email fct@menara.ma , Secretariat email bouchra@par3com.com

 
This recent study Padova, Italy ( Orzan & Mungia, Int J Pediatr Otorhinolaryngol. 2007 Jan 10;.) studied 79 children with genetically diagnosed  Connexin 26 hearing loss and observed that over half of these had normal hearing at age 3 months

Abstract:

Hearing loss associated with mutations of the GJB2, the gene encoding Connexin 26 (Cx26), is described as a prelingual, bilateral, prevalently stable sensorineural defect ranging in severity from mild to profound. Despite many clinical studies, there is still a limited knowledge about the severity of Cx26 hearing loss at birth, in the postnatal period or in early infancy; some authors have reported about a possible variable age of onset. The aim of this work was to investigate the characteristics of Cx26 hearing loss and test the hypothesis of a postnatal sudden and severe deterioration of the hearing capacity in cases with uncertain age at onset. METHODS: We have studied 79 children with molecularly documented biallelic Cx26 hearing loss by evaluating longitudinal audiometric characteristics and the results of a questionnaire administered to the parents, regarding the auditory behavior of their children at 3 and 6 months of age. RESULTS: More than 50% of children with profound hearing loss were described as having normal auditory behavior at three months of age, and at least 20% of these children were consistently reported by the parents to maintain normal auditory development up to 6 months of age. None of the studied children showed significant progression in hearing loss from the time of diagnosis through their last follow-up. In a few cases these reports were supported by objective audiometric evaluations. CONCLUSIONS: Based on these data, we hypothesize that Cx26 profound hearing loss may be not always congenital, with the possibility of an early window of "functional time" before the final defect is established. The hypothesis of an early auditory input makes timing of detection and intervention critical to minimize the deleterious effects of a functional deprivation. In a near future, the combination of genetic testing with universal neonatal hearing screening and audiological surveillance will provide invaluable information about the natural history of the most frequent sensory defect in infancy and will consequently allow to maximize the quality of intervention.

 


     Journal Watch :Falls among institutionalized elderly in Alexandria. Makhlouf MM & Ayoub AI, 2000

 1.   DODA 2006, capable of advanced hearing measure, and also paediatric hearing assessment is being developed. If you requested for and got a free copy of DODA, you may also look out for this latest version dubbed DODA-i, as well as for an additional page on outcome of hearing assessment using DODA.

 2.  From  http://www.otolaryngologyinafrica.net/grandround/  is a new addition - a recent conference poster presentation. This presentation is available at http://www.otolaryngologyinafrica.net/grandround/archive.htm .

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 Till Next Week, Welcome to 2007!

 Biodun

 

 

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                          © Copyright Dr 'Biodun Olusesi,  2005 - 2007

 

 Molecular Biology of Head & Neck Cancer