Plasma exchange in the treatment of Refsum's disease (heredopathia atactica polyneuritiformis).
نویسندگان
چکیده
Five cases of heredopathia atactica polyneuritiformis (HAP--Refsum's disease) were treated by serial plasma exchanges. In all patients a reduction in calorie intake and body weight had been associated with a rise in plasma phytanic acid, followed by an exacerbation of the ataxia and neuropathy. Lowering the plasma phytanic acid by plasma exchange produced a rapid clinical improvement. The main indication for plasma exchange in HAP is a severe or rapidly worsening clinical condition. A lesser indication is failure of dietary management to reduce a high plasma phytanic acid level.
منابع مشابه
The significance of plasma phytanic acid levels in adults.
The presence of phytanic acid in tissues and plasma has been considered diagnostic of heredopathia atactica polyneuritiformis (Refsum's disease), but recently slightly raised plasma phytanic acid levels have been reported in other conditions. Forty two normal people were found to have a phytanic acid level of 0-33 mumol/l. Fourteen patients with heredopathia atactica polyneuritiformis had a pla...
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This paper describes a diabetic child showing most of the features of a condition described by Refsum (Refsum, 1945, 1946a and 1946b, 1948, 1952; Refsum, Salomonsen and Skatvedt, 1949) under the name of heredopathia atactica polyneuritiformis. The malady is thought to be a recessive condition and is usually referred to as Refsum's syndrome. Only six other cases have so far been reported (Reese ...
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A female patient started to develop deafness and vertigo at the age of 29. In the following years she became atactic and retinitis pigmentosa was discovered. The diagnosis of Refsum's disease was reached on the grounds of the high concentration of phytanic acid in plasma. The patient died 23 years after onset of the first symptoms. Liver, spleen and kidney showed lipofuscinosis and pigment-lade...
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Thirty-nine cases of Refsum's syndrome (Refsum, 1946) or heredopathia atactica polyneuritiformis have now been reported (Carrell et al., 1966). The neurological features-namely, a mixed sensory and motor peripheral neuropathy, atypical retinitis pigmentosa with night blindness and constricted visual fields, cerebellar ataxia, and nerve deafness-are well attested and have been recently reviewed ...
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عنوان ژورنال:
- Journal of neurology, neurosurgery, and psychiatry
دوره 54 7 شماره
صفحات -
تاریخ انتشار 1991