Acquired Synesthesia in Retinitis Pigmentosa
نویسندگان
چکیده
Patient PH developed retinitis pigmentosa in childhood and progressively lost his vision until he became completely blind at 40 years old. At age 42, he started experiencing vivid ‘synesthesia’; tactile stimuli on the hand evoked a vivid visual sensation of ‘movement’, ‘expansion’ or ‘jumping’. Intriguingly, the synesthesia was much more vivid when the hand was in front of the face rather than behind. The effect is unlikely to be confabulatory since touch thresholds (Semmes Monofilaments) were normal and identical for hand in front versus hand behind the head, while ‘thresholds’ for evoked visual sensations were significantly higher for the ‘behind’ condition. Also, the critical fusion frequency for the tactile sensation was much higher than the visually evoked ones. We propose three explanations. (i) ‘Remapping’ or ‘cross-talk’. As a result of de-afferentation, sensory input to the somatosensory pathways (e.g. insular cortex) also innervates extrastriate visual areas. (ii) When a person is touched, there may be spontaneously evoked tactile associative ‘memories’ that would not normally evoke actual visual qualia because of competing ‘spontaneous activity’ from the visual pathways. However, upon de-afferentation, the associations may be experienced as synesthesia. (iii) After de-afferentation, the ‘back projections’ to somatosensory areas from visual areas may be strengthened.
منابع مشابه
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 کاملشب 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 کاملCauses 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 کاملStudy 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 کاملGenetic markers for retinitis pigmentosa.
OBJECTIVE To review recent advances in the molecular genetics of retinitis pigmentosa with emphasis on the development of genetic markers that aids diagnosis and prognosis. DATA SOURCES AND EXTRACTION Literature search of MEDLINE from 1988 to 2005 using the following key words: 'retinitis pigmentosa', 'rhodopsin', 'RP1', 'RPGR', and 'genetic counseling'. References of two genes--RHO and RP1--...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 1999