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 evaluat...
Achondroplasia is a relatively common genetic skeletal dysplasia that manifests with stunted stature...
SummaryTemporal bone osteodysplasia can produce many different symptoms, such as involvement restric...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
The goal of this review is to evaluate the management options for achondroplasia, the most common no...
The goal of this review is to evaluate the management options for achondroplasia, the most common no...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skel...
INTRODUCTION: In children, hypoacusis, or conductive hearing loss, is usually acquired; otitis med...
SummaryOtospongiosis is an osteodystrophy of the temporal bone, characterized by disordered neoforma...
Abstract Background Fibrous dysplasia is a slowly progressive benign fibro-osseous disorder that inv...
Facio-audio-symphalangism syndrome is a rare autosomal dominant genetic disorder with characteristic...
Achondroplasia is a relatively common genetic skeletal dysplasia that manifests with stunted stature...
SummaryTemporal bone osteodysplasia can produce many different symptoms, such as involvement restric...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
The goal of this review is to evaluate the management options for achondroplasia, the most common no...
The goal of this review is to evaluate the management options for achondroplasia, the most common no...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
A review of numerous case reports was made, in order to demonstrate the possibilities for treatment ...
Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skel...
INTRODUCTION: In children, hypoacusis, or conductive hearing loss, is usually acquired; otitis med...
SummaryOtospongiosis is an osteodystrophy of the temporal bone, characterized by disordered neoforma...
Abstract Background Fibrous dysplasia is a slowly progressive benign fibro-osseous disorder that inv...
Facio-audio-symphalangism syndrome is a rare autosomal dominant genetic disorder with characteristic...
Achondroplasia is a relatively common genetic skeletal dysplasia that manifests with stunted stature...
SummaryTemporal bone osteodysplasia can produce many different symptoms, such as involvement restric...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...