An autosomal recessive familial disorder that usually presents in childhood with POLYNEUROPATHY; SENSORINEURAL HEARING LOSS; ICHTHYOSIS; ATAXIA; RETINITIS PIGMENTOSA; and CARDIOMYOPATHIES. (From Joynt, Clinical Neurology, 1991, Ch37, p58-9; Rev Med Interne 1996;17(5):391-8) This condition can be caused by mutation in the genes encoding peroxisomal phytanoyl-CoA hydroxylase or proteins associated peroxisomal membrane, leading to impaired catabolism of PHYTANIC ACID in PEROXISOMES.

Descriptor ID	D012035
MeSH Number(s)	C10.228.140.163.100.680.760 C10.500.300.780 C10.574.500.495.780 C10.668.829.800.300.780 C16.131.666.300.780 C16.320.400.375.780 C16.320.565.189.680.760 C16.320.565.663.760 C18.452.132.100.680.760 C18.452.648.189.680.760 C18.452.648.663.760
Concept/Terms	Refsum Disease Refsum Disease Disease, Refsum Hereditary Motor And Sensory Neuropathy Iv Hereditary Motor and Sensory Neuropathy, Type IV Hereditary Type IV Motor and Sensory Neuropathy Heredopathia Atactica Polyneuritiformis Polyneuritiformis, Heredopathia Atactica HMSN 4 HMSN Type IV Neuropathy, Hereditary Motor and Sensory, Type IV Phytanic Acid Oxidase Deficiency Phytanic Acid Storage Disease Refsum Disease, Adult Adult Refsum Disease Adult Refsum Diseases Disease, Adult Refsum Diseases, Adult Refsum Refsum Diseases, Adult Refsum Disease, Classic Classic Refsum Disease Classic Refsum Diseases Disease, Classic Refsum Diseases, Classic Refsum Refsum Diseases, Classic Refsum's Disease Disease, Refsum's Refsums Disease Refsum's Syndrome Refsum Syndrome Refsums Syndrome Syndrome, Refsum's Refsum-Thiebaut Syndrome Refsum Thiebaut Syndrome Refsum-Thiebaut Syndromes Syndrome, Refsum-Thiebaut Syndromes, Refsum-Thiebaut HMSN IV HMSN IVs Hemeralopia Heredoataxia Polyneuritiformis Heredoataxia Polyneuritiformis, Hemeralopia Polyneuritiformis, Hemeralopia Heredoataxia Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency Refsum Disease, Phytanoyl CoA Hydroxylase Deficiency Refsum Disease, Phytanic Acid Oxidase Deficiency

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