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Heredopathia atactica polyneuritiformis (phytanic acid storage disease). A new case with special reference to dietary treatment.

作者信息

Sahgal V, Olsen W O

出版信息

Arch Intern Med. 1975 Apr;135(4):585-7.

PMID:49180
Abstract

A 33-year-old man with Refsum disease exhibited clinical features of night blindness, dysequilibrium, hearing loss, itchy dry skin, symmetrical polyneuropathy, distal muscle weakness, pes cavus, and hammer toe. His total serum protein was increased, nerve conduction velocities were slow, and serum phytanic acid levels were high. Dietary restriction of phytol resulted in a decrease in serum phytanic acid without any visual and autitory changes; however, coordination, skin lesions, and nerve conduction velocities definitely improved.

摘要

相似文献

1
Heredopathia atactica polyneuritiformis (phytanic acid storage disease). A new case with special reference to dietary treatment.
Arch Intern Med. 1975 Apr;135(4):585-7.
2
[Heredopathia atactica polyneuritiformis. Hexadecanoic acid storage disease (Refsum's disease). Definition, treatment and pathogenesis. A short review].[遗传性共济失调性多神经炎样病。十六烷酸贮积病(雷夫叙姆病)。定义、治疗与发病机制。简要综述]
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Heredopathia atactica polyneuritiformis (Refsum's Disease): a second trial of dietary therapy in two patients.
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[Refsum syndrome, heredopathia atactica polyneuritiformis in the view of the otolaryngologist (author's transl)].从耳鼻喉科医生的角度看雷夫叙姆综合征(遗传性共济失调性多神经炎)(作者译)
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Heredopathia atactica polyneurotiformis: therapeutic and pathogenetic aspects.
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[Refsum's syndrome (author's transl)].[雷夫叙姆综合征(作者译)]
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Heredopathia atactica polyneuritiformis phytanic-acid storage disease, Refsum's disease:" a biochemically well-defined disease with a specific dietary treatment.遗传性共济失调性多神经炎样病、植烷酸贮积病、雷夫叙姆病:一种生化特征明确且有特定饮食疗法的疾病。
Arch Neurol. 1981 Oct;38(10):605-6. doi: 10.1001/archneur.1981.00510100033003.
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[Clinical and biochemical follow up of Refsum's disease (author's transl)].雷夫叙姆病的临床与生化随访(作者译)
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9
[Heredopathia atactica polyneuritiformis: phytanic acid storage disease (Refsum's syndrome). Effect of diet therapy on retinal and cochlear changes].[遗传性共济失调性多神经炎型:植烷酸贮积病(雷夫叙姆综合征)。饮食疗法对视网膜和耳蜗变化的影响]
Neurol Neurochir Pol. 1984 Jan-Feb;18(1):1-4.
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[Phytanic-acid storage disease: Refsum's syndrome. Heredopathia atactica polyneuritiformis].[植烷酸贮积病:雷夫叙姆综合征。遗传性共济失调性多神经炎]
Dtsch Med Wochenschr. 1977 Oct 14;102(41):1480-4. doi: 10.1055/s-0028-1105516.

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Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.夏科-马里-图思病是否应根据运动传导速度进行基因亚组分类。
J Neurol Neurosurg Psychiatry. 1982 Feb;45(2):182-4. doi: 10.1136/jnnp.45.2.182.
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J Neurol Neurosurg Psychiatry. 1982 Dec;45(12):1085-91. doi: 10.1136/jnnp.45.12.1085.
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Case report 175: Refsum syndrome.
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3-Methyladipate excretion in animals fed a phytol supplement with reference to Refsum's disease.以Refsum病为参照,研究喂食叶绿醇补充剂的动物中3-甲基己二酸的排泄情况。
J Inherit Metab Dis. 1985;8 Suppl 2:147-8. doi: 10.1007/BF01811502.