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Diagnosis of osteopetrosis in bilateral congenital aural atresia: Turning point in treatment strategy
Author(s) -
Ritu Verma,
Manisha Jana,
Ashu Seith Bhalla,
Arvind Kumar,
Rakesh Kumar
Publication year - 2016
Publication title -
world journal of clinical pediatrics
Language(s) - English
Resource type - Journals
ISSN - 2219-2808
DOI - 10.5409/wjcp.v5.i2.228
Subject(s) - medicine , dysplasia , atresia , osteopetrosis , microtia , conductive hearing loss , auditory canal , hearing loss , temporal bone , middle ear , surgery , audiology , pathology
Aural atresia is a rare congenital malformation of the external and middle ear. There are several syndromic associations of this anomaly with those involving the first and second branchial arches. Occurrence of aural atresia with sclerosing skeletal dysplasia is unknown and has never been reported. The co-existence of a sclerosing dysplasia can make the surgical treatment in aural atresia difficult and risky; and the auditory improvement may not be as expected. Moreover, internal auditory canal narrowing and hence sensorineural hearing loss in sclerosing dysplasia might add to the already existing conductive hearing loss in such patients. In this case report we have described an unknown association of bilateral microtia with sclerosing skeletal dysplasia (autosomal dominant osteopetrosis) and clinical implications of these two conditions occurring together leading to a change in the management plan.

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