Audiometric and vestibular examinations in retinitis pigmentosa.

نویسندگان

  • J LANDAU
  • M FEINMESSER
چکیده

DEAFNESS is one of the most frequent degenerative processes associated with retinitis pigmentosa (Duke-Elder, 1940; Fowler, 1947), the frequency being variously reported as between 2 and 43 per cent. (Azzolini and Cortesi, 1951). These variations in the incidence in different series may be due to the diversity of methods employed to measure hearing and different criteria in evaluating the degree of impairment. Since the introduction of audiometry as a routine method of measuring hearing loss, the number of reports of affected hearing audiometrically examined in many diseases has greatly increased. In retinitis pigmentosa however, the reported cases which have been examined audiometrically were almost always in small series (Sirles and Slaughter, 1943; Givner and Bruger, 1947; Azzolini and Cortesi, 1951; dell'Acqua, 1952; Bietti, 1952; Alagna and Nizetic, 1953; Lavalle, 1953). During the past 3 years it has been possible to perform audiometric tests on a number of patients and vestibular tests in over half of them. The results of this study are now presented.

برای دانلود رایگان 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

Study of Patterns of Inheritance in Affected Patients with Retinitis Pigmentosa in Iranian Populations

Background and Aims: Retinitis pigmentosa (RP) is the most common form of inherited retinal degeneration, photoreceptors loss of which in the retina causes visual loss. The purpose of the present study was to determine patterns of inheritance in RP patients in Yazd to help the health professional for designing suitable laboratory testing for the high risk families. Materials and Methods: Thirt...

متن کامل

Simultaneous Presence of Macular Corneal Dystrophy and Retinitis Pigmentosa in Three Members of a Family

Macular corneal dystrophy (MCD) is an autosomal recessive hereditary disease. In most cases, various mutations in carbohydrate sulfotransferase 6 (CHST6) gene are the main cause of MCD. These mutations lead to a defect in keratan sulfate synthesis. Retinitis pigmentosa (RP) is another eye disorder with nyctalopia as its common symptom. It has been shown that more than 65 genes have been implica...

متن کامل

شب کوری، هتروکرومیا و یووئیت در یک فرد از سلسله بیماران شب‌کور

   The classical clinical triad of retinitis pigmentosa is arteriolar attenuation , retinal bone-spicule pigmentation and waxy disc pallor.   A 33 year old female patient is introduced here. She had unilateral posterior subcapsular cataract, heterochromic iris, and uveitis.The patient also suffered night blindness , had a family history of low vision ,and reduced visual acuity in her right e...

متن کامل

Causes of Childhood Blindness among Students of Blinds' School in Shiraz, Iran

Background: Causes of blindness in children vary according to the region and socioeconomic development. Within a given country these causes vary with passage of time. This reflects different levels of socioeconomic development and provision of healthcare services. This cross-sectional study was undertaken to estimate the major causes of severe visual impairment in children and specially prevent...

متن کامل

[Unilateral retinitis pigmentosa or pseudoretinitis pigmentosa? Case report].

Unilateral retinitis pigmentosa is a rare disease characterized by loss of photoreceptors and retinal pigment deposition without affecting the contralateral eye. Although described more than one hundred years its existence is still questioned. This article reports a case of a patient with abnormalities suggestive of unilateral retinitis pigmentosa. The clinical and complementary examinations ar...

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

عنوان ژورنال:
  • The British journal of ophthalmology

دوره 40 1  شماره 

صفحات  -

تاریخ انتشار 1956