Speech-language pathology aspects in a pediatric case of head and neck arthrogryposis

被引：1

作者：

Tribdade, Jennifer Alvares ^{[1
]}

Freitas, Jordana da Silva ^{[1
]}

Menzen, Liliane ^{[1
]}

Laux, Carolina ^{[1
]}

Barbosa, Lisiane de Rosa ^{[1
]}

de Almeida Freitas Cardoso, Maria Cristina ^{[1
]}

机构：

[1] UFCSPA, Porto Alegre, RS, Brazil

来源：

CODAS | 2018年 / 30卷 / 02期

关键词：

Arthrogrposis; Syndrome; Deglutition Disorder; Speech-language and Hearing Sciences; Child;

D O I：

10.1590/2317-1782/20182017181

中图分类号：

R36 [病理学]; R76 [耳鼻咽喉科学];

学科分类号：

100104 ; 100213 ;

摘要：

Arthrogryposis is a rare, multiple, congenital syndrome anon-progressive nature characterized by a series of genetic malformations, as well as stiffness and joint contractures. This is a clinical case study whose objective is to describe speech-language pathology disorders through the evaluation process in a case olarthrogryposis in Pediatrics. The medical records or a patient were analyzed from birth. A complete clinical evaluation o f pediatric dysphagia was performed, establishing a diagnosis of severe oropharyngeal dysphagia evidenced by functional and structural impairments. Hearing loss was detected in association with this condition.

引用

页数：4

共 15 条

[1]

Azevedo MF, 1991, ACTA AWHO, V10, P107

[2] Oropharyngeal Dysphagia in Children Mechanism, Source, and Management [J].