ABSTRACT Congenital deafness affects the speech and psychosocial development of the affected child. It could be syndromic or non-syndromic depending on the presence or absence of the associated manifestations. Among various etiological factors described for deafness, consanguinity is an established high risk etiological factor. A prospective study was carried out in 1076 children in the age group of 0-14years attending Government ENT hospital and schools for deaf in and around Hyderabad. The results showed that 41.73 % (449) of the cases were the products of consanguineous matings and 58.27 % (627) were born to non consanguineous parents. Further analysis revealed a high rate of consanguinity (44.53%) in children with non syndromic deafness
Background and purpose: Hearing impairment as a heterogeneous disorder is the most common sensory de...
The deaf child\u27s history is broken down into his family history, his prenatal history, his delive...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...
Abstract Introduction: Estimates of the magnitude of consanguinity related profound bilateral senso...
Consanguineous marriage is strongly favored in many large human populations. In the most parts of so...
Background: Deafness is the hidden disability of childhood, and leads to poor educational and employ...
Introduction: Sensorineural hearing loss (SNHL) accounts for about 60% of all hearing loss. This is ...
Objective: To find out the frequency of consanguinity and positive family history of hearing impairm...
Background: Hearing toss (HL) and its complications appear to be increasingly common in developing c...
Recent advances in molecular genetics have allowed the determination of the genetic cause of some ch...
Objectives: The prevalence of consanguineous marriage is about 30 % in Iran and this can increase th...
The purpose of this paper is to study the prevalence rate of hearing impairment among children with ...
PubMed ID: 12122638OBJECTIVES: This study aimed to determine the severity, age of presentation, and ...
Abstract Introduction: Wedlock is beneficial when a couple is hesitant to meet the societal ideal o...
Background: We report on the higher prevalence of deaf-mutes from a village in Jammu and Kashmir Sta...
Background and purpose: Hearing impairment as a heterogeneous disorder is the most common sensory de...
The deaf child\u27s history is broken down into his family history, his prenatal history, his delive...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...
Abstract Introduction: Estimates of the magnitude of consanguinity related profound bilateral senso...
Consanguineous marriage is strongly favored in many large human populations. In the most parts of so...
Background: Deafness is the hidden disability of childhood, and leads to poor educational and employ...
Introduction: Sensorineural hearing loss (SNHL) accounts for about 60% of all hearing loss. This is ...
Objective: To find out the frequency of consanguinity and positive family history of hearing impairm...
Background: Hearing toss (HL) and its complications appear to be increasingly common in developing c...
Recent advances in molecular genetics have allowed the determination of the genetic cause of some ch...
Objectives: The prevalence of consanguineous marriage is about 30 % in Iran and this can increase th...
The purpose of this paper is to study the prevalence rate of hearing impairment among children with ...
PubMed ID: 12122638OBJECTIVES: This study aimed to determine the severity, age of presentation, and ...
Abstract Introduction: Wedlock is beneficial when a couple is hesitant to meet the societal ideal o...
Background: We report on the higher prevalence of deaf-mutes from a village in Jammu and Kashmir Sta...
Background and purpose: Hearing impairment as a heterogeneous disorder is the most common sensory de...
The deaf child\u27s history is broken down into his family history, his prenatal history, his delive...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...