Otosclerosis (Q42107): Difference between revisions

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Otosclerose é uma doença óssea metabólica geneticamente mediada que afeta a cápsula ótica e o estribo. É um transtorno autossômico dominante com penetrância e expressividade variáveis. Geralmente, a perda auditiva sintomática por otosclerose se desenvolve no início da terceira década de vida, embora início na adolescência ocorra.
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Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomatic hearing loss from otosclerosis develops early in the third decade of life, although onset in the teenage years does occur.

Revision as of 08:31, 13 August 2026

Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomatic hearing loss from otosclerosis develops early in the third decade of life, although onset in the teenage years does occur.
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    English
    Otosclerosis
    Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomatic hearing loss from otosclerosis develops early in the third decade of life, although onset in the teenage years does occur.

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