SciELO - Scientific Electronic Library Online

 
vol.27 número3Trissomia 20 em mosaico: um fenótipo subtilA influência de fatores socioculturais no conteúdo dos delírios, delírio futebolístico: dois casos clínicos índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Nascer e Crescer

versión impresa ISSN 0872-0754versión On-line ISSN 2183-9417

Resumen

PINTO, Ana Nóbrega; COUTINHO, Miguel Bebiano; SOARES, Teresa  y  SOUSA, Cecília Almeida. Acromicric dysplasia and hearing loss: A case report. Nascer e Crescer [online]. 2018, vol.27, n.3, pp.185-187. ISSN 0872-0754.  https://doi.org/10.25753/BirthGrowthMJ.v27.i3.13190.

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 reported. However, little is known about the otolaryngologic aspects that may accompany this disease. We pretend to raise awareness to the otolaryngologic aspects that may accompany acromicric dysplasia and to the possible interventions that improve these patients quality of life. Clinical Case: We present the case of a ten-year-old girl referred to the otorhinolaryngology consultation with complaints of progressive hearing loss. Hearing evaluation confirmed bilateral severe mixed hearing loss and the patient was successfully rehabilitated with bone-anchored hearing aids. Discussion/Conclusions: Evaluation by an otolaryngologist should be part of the management of children with bone dysplasias, especially if they present with associated symptoms, to allow an early diagnosis and proper intervention.

Palabras clave : Bone dysplasias; hearing loss; hearing impairment rehabilitation.

        · resumen en Portugués     · texto en Inglés     · Inglés ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons