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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Detalhes bibliográficos
Autor principal: Pinto, Ana Nóbrega (author)
Outros Autores: Coutinho, Miguel Bebiano (author), Soares, Teresa (author), Sousa, Cecília Almeida (author)
Formato: article
Idioma:eng
Publicado em: 2018
Assuntos:
Texto completo:https://doi.org/10.25753/BirthGrowthMJ.v27.i3.13190
País:Portugal
Oai:oai:ojs.revistas.rcaap.pt:article/13190