[Psychogenic deafness in children--audiological characteristics].

نویسنده

  • F Kudoh
چکیده

During the period from 1980 to 1984, 50 cases (98 ears) of psychogenic deafness in children have been examined at the hearing clinic of the Department of Otolaryngology. All were school children aged from 6 to 15 years. They were classified into 3 groups (A, B, C) and their audiological, psychological, opthalmological findings and progress were reported. Cases of A group complained of deafness and consulted specialists of their own accords. Cases of B group have complained of symptom of ear, but consulted a doctor after screening audiometry and cases of C group have had no symptom of hearing trouble. Their audiological findings were the bilateral perceptive flat loss type, usually lying between 40 to 100 dB. Results of speech discrimination test were usually better than that of pure tones. A half of them revealed type V of Bekesy audiometry. There were unexplainable discrepancy between the threshold of pure tone audiometry and response threshold of ERA.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Psychogenic Vomiting: A Clinical Diagnosis Merits Special Attention in Pediatrics

A 2 years and 9 months old boy attended to a gastroenterology clinic of pediatric hospital for investigation of recurrent and intractable vomiting. He had post prandial, non-projectile, non-bilious emesis since past 2 years. Since the onset of illness, he was carried to many doctors and underwent extensive laboratory investigations. Because all of the science lab and imaging work up for etiolog...

متن کامل

Genetic characteristics in children with cochlear implants and the corresponding auditory performance.

OBJECTIVES/HYPOTHESIS To explore the genetic characteristics of children with cochlear implants (CIs) and to correlate the auditory performance after implantation to the genetic diagnosis of children with CIs. STUDY DESIGN Prospective cohort study. METHODS Mutations of four common deafness-associated genes, GJB2, SLC26A4, the mitochondrial 12S rRNA gene, and OTOF, were screened in 743 unrel...

متن کامل

Cochlear implantation in adults with prelingual deafness. Part II. Underlying constraints that affect audiological outcomes.

OBJECTIVES/HYPOTHESIS To discuss the underlying physiological and anatomical constraints on audiological performance of late-implanted prelingually deafened adult cochlear implant patients. STUDY DESIGN Retrospective review. METHODS Published literature on the topic of auditory pathway responses to prolonged congenital deafness was reviewed. In particular, the authors sought to identify the...

متن کامل

Analysis of p.V37I compound heterozygous mutations in the GJB2 gene in Chinese infants and young children.

The p.V37I (c.109G>A) mutation in the GJB2 gene is the common frequent cause of congenital deafness; however, its pathogenicity is debated. The present study investigated the prevalence of p.V37I in Chinese infants and young children and associated clinical characteristics. The subjects of the present study were screened for mutations in GJB2 (235delC, 299delAT, 176dell6, 35delG), SLC26A4 (IVS7...

متن کامل

Simultaneous nonepileptic spells and nonorganic hearing loss: A case of comorbid psychogenic symptoms☆

A twenty-eight-year-old woman with an eight-year history of partial hearing loss presented with a two-year history of worsening deafness and new-onset seizures. Evaluations of tympanic membranes, cochlea, and auditory brain stem reflexes demonstrated no physiologic basis for deafness. Video-EEG monitoring demonstrated that the patient responded normally to spontaneous auditory stimuli and that ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Nihon Jibiinkoka Gakkai kaiho

دوره 88 11  شماره 

صفحات  -

تاریخ انتشار 1985