Speech development in children of preschool age with arthrogryposis multiplex congenital with upper limb deformities

Author:

Agranovich Olga E.ORCID,Agranovich Zoya E.ORCID,Ermolovich Evgeniya I.ORCID,Petrova Ekaterina V.ORCID,Iskandarov Ildar R.ORCID,Ivanov Dmitry A.ORCID,Shestakova Anna N.,Blagoveschenskiy Evgeniy D.ORCID

Abstract

BACKGROUND: The difficulties or gross disturbance in motor development, which are diagnosed in children at an early age, are one of the prognostic markers of further problems in their speech development. AIM: This study aimed to determine the speech development of children with arthrogryposis multiplex congenita with upper limb deformities. MATERIALS AND METHODS: Speech examination was conducted in 21 children with arthrogryposis multiplex congenita preschool age (average age: 5.16 1.49 years) from 2020 to 2021. Patients were divided into 2 groups: group 1 (10 people) with children of younger and middle preschool age (average age 3.81 0.63 years) and group 2 (11 people) with children of older and preparatory preschool age (average age 6.39 0.78 years). The speech examination results were exposed to statistical analysis. RESULTS: The majority of children with arthrogryposis multiplex congenita had speech pathology (90.5%), whereas general speech underdevelopment dominated over speech development delay (78.9% and 21.1%, respectively). A high frequency of perinatal hypoxic-ischemic encephalopathy in children with arthrogryposis multiplex congenita (80.9%), a complicated perinatal anamnesis (57.1%), and a delay in early motor or speech development (100% and 52.4%, respectively) links with speech disorder development in the future. Patients with arthrogryposis have a large percentage of congenital pathology of the articulatory apparatus structure (57.1%). Of the children, 76.2% were with a total form of arthrogryposis multiplex congenita, whereas 23.8% with an isolated upper extremity lesion. No statistically significant differences were determined in the form of speech pathology between patients with various forms of arthrogryposis multiplex congenita. Children of the first age group had speech disorders in 90% of cases, whereas 90.9% in group 2. Based on the form of speech pathology, patients with general speech underdevelopment and speech development delay were determined in group 1 (55.6% and 44.4%, respectively), whereas children with general speech underdevelopment in group 2 (100%). In the clinical form of speech pathology, dysarthria prevailed in children of both age groups (80%). CONCLUSIONS: Children with arthrogryposis multiplex congenita with upper limb deformities have a high incidence of speech disorders. Early speech examination and speech therapy eliminated all detected disturbances.

Publisher

ECO-Vector LLC

Subject

Orthopedics and Sports Medicine,Surgery,Pediatrics, Perinatology and Child Health

Reference47 articles.

1. International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita

2. Antúnez NH, González C, Cerisola F, et. al. Artrogriposis múltiple congénita: Análisis de los pacientes asistidos en el Centro de Rehabilitación Infantil Teletón. Uruguay Rev Med Urug. 2015;31(1):27−31.

3. Cuevas G, Cognian C. Artrogriposis multiple congenita. En: Blanco M. Enfermedades invalidantes de la infancia: enfoque integral de rehabilitacion. Santiago de Chile: Teleton; 2006:128−133.

4. Amyoplasia revisited

5. Macias Merlo L, Fagoaga Mata J. Fisioterapia en pediatria. Madrid: McGraw-Hill/Interamericana, 2002:235−251.

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