Acromicric dysplasia and hearing loss: A case report

Introduction: Acromicric dysplasia is an extremely rare autosomal dominant bone dysplasia characterized by progressive growth retardation, short hands and feet, mild facial dysmorphism and generalized joint limitation. Association with ear, nose and pharyngolaryngeal alterations has been previously...

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Bibliographic Details
Main Author: Pinto, Ana Nóbrega (author)
Other Authors: Coutinho, Miguel Bebiano (author), Soares, Teresa (author), Sousa, Cecília Almeida (author)
Format: article
Language:eng
Published: 2018
Subjects:
Online Access:https://doi.org/10.25753/BirthGrowthMJ.v27.i3.13190
Country:Portugal
Oai:oai:ojs.revistas.rcaap.pt:article/13190