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Updated: Dec 4, 2025

Systematic Hearing Performance Evaluation Process for Adolescents with Cochlear Implantation at Early Ages
Published on: March 24, 2023
Precochlear Implant Assessment: Clinical Profile and Family History of Children with Severe Bilateral Prelingual
Syed Hashim Raza1, Rehmana Waris1, Samina Akhtar2
1Children Hospital, Pakistan Institute of Medical Sciences, Islamabad, Islamabad, Pakistan.
Insights
Consanguineous marriage is common in Pakistani children with profound hearing loss, often linked to language impediments and developmental delays. Early consultation is crucial for their development.
Area of Science:
- Pediatrics
- Genetics
- Public Health
Background:
- High prevalence of deafness in Pakistan necessitates understanding clinical features for effective public health interventions.
- Clinical insights into profound hearing loss aid in identifying causes and planning strategic health initiatives.
Purpose of the Study:
- To detail clinical aspects of children with profound hearing loss, including age at presentation, associated deficits, causes, family history, and the role of consanguineous marriage.
- To investigate the relationship between consanguineous marriage patterns and the occurrence of hearing loss in children.
Main Methods:
- Study conducted from November 2016 to September 2018, including children under 6 with profound bilateral hearing loss.
- Utilized Schedule of Growing Skills II for developmental assessment and detailed family history collection.
- Statistical analysis performed using SPSS version 20.0.
Main Results:
- Mean age of treated children was 3.2 ± 1.25 years.
- A positive family history was reported in 51.5% of patients, with 76.9% having consanguineous parents (first-degree relatives).
- Language impediments affected 90.8% of patients; 3.07% had global developmental delay.
Conclusions:
- Consanguineous marriage patterns significantly contribute to hereditary diseases, including hearing loss, in families.
- Children's developmental progress is closely associated with their age at the time of medical consultation.
Abstract:
Introduction The prevalence of deafness is high in Pakistan. Knowledge regarding the clinical features of patients with profound hearing loss will not only help identify the cause but will also help in the strategic planning for public health interventions. Objective The present study was conducted to cover in detail the clinical aspects of children with hearing loss, that is, age at presentation, associated deficits and disorders, possible cause of the disease, associated family history, and role of consanguineous marriage. Methods The present study was performed from November 2016 to September 2018. All of the patients under 6 years of age with profound bilateral hearing loss who would benefit from cochlear implantation were included in the study. Detailed history was taken. The developmental skills were assessed for all areas, and the patients were scored regarding their motor, manipulative, visual, language, social and self-care skills according to the Schedule of Growing Skills II. Detailed family history was taken from the parents of the affected children. The Statistical Package for the Social Sciences (SPSS) software, version 20.0, was used for the statistical analysis. Results The mean age of the children to be treated was 3.2 ± 1.25 years. Most patients (51.5%) had a positive family history of disease. Consanguineous marriage was common; the parents of 76.9% of the patients were first-degree relatives. Most patients (90.8%) had associated language impediments. In total, four (Ł3.07%) patients had global developmental delay. Conclusion Consanguineous marriage pattern plays an important role in diseases running in families. Development in these children is strongly linked to their age at the consultation.
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