Differential (Click to cross reference) Addison's disease adrenoleukodystrophy adrenoleukodystrophy, adult onset adrenoleukodystrophy, carrier adrenomyeloneuropathy adverse drug reaction affect, inappropriate aminoacidopathies arrhythmia, cardiac ataxia ataxic gait Bassen-Kornzweig syndrome blindness bone marrow transplantation cataracts cataracts, congenital cerebro hepato renal syndrome cerebrovascular accident children chorea clubfoot as related to neurologic disease Cockayne's syndrome congenital heart disease congenital malformation cortical blindness crying, pathologic cultured skin fibroblasts deafness decerebrate posture dementia dementia, childhood demyelinating disease diet disability, neurological DNA probes drug induced neurologic disorders dysarthria dysmorphic dysphagia dystonia electrocardiogram, abnormal electronystagmography electroretinograph enzyme, defect epidemiology of neurology episodic neurologic deficits exercise intolerance failure to thrive familial fatty acid, elevated plasma content foot deformity fundus, abnormality of gender gene gene therapy genetic counselling genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic testing Hallervorden Spatz disease hearing loss hepatomegaly hyperpigmentation of skin hypogonadism hypotonia inborn errors of metabolism intellectual deterioration Kearns-Sayre syndrome kyphoscoliosis, neurologic causes of lactic acidemia Laurence-Moon-Bardet-Biedl syndrome leukodystrophy Lorenzo's oil lysosomal storage disease macular degeneration malformation, CNS, congenital mental retardation metabolic disorder, primary misdiagnosis motor neuron disease MRI MRI, abnormal mucopolysaccharidoses muscle atrophy, progressive muscle weakness myopathy, mitochondrial myopia nasal bridge, wide neurologic disease neurologic disease, diagnoses of neurologic signs neurologic testing neuronal ceroid-lipofuscinosis neuropathy neuropathy, ataxic neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, onion bulb night blindness optic atrophy optic nerve optic neuropathy paraparesis, spastic paroxysmal neurologic deficits peroxisomal disease peroxisomes personality change pes cavus phytanic acid pigmentary retinopathy polyneuropathy prenatal diagnosis by amniocentesis prognosis pseudobulbar palsy psychiatric problems in neurologic disorders psychomotor retardation quadriparesis refractive errors Refsum's disease retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article seizure seizure, neonatal sensorineural hearing loss sensory loss skin, darkening of skin, lesions in neurologic disorders spinocerebellar degeneration sudden death tapetoretinal degeneration testicular atrophy treatment of neurologic disorder urea-cycle enzymopathies Usher's syndrome very long chain fatty acids visual field defect visual fields, constricted visual loss weakness white matter disease

Showing articles 0 to 10 of 10 Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 MR of Zellweger Syndrome AJNR 18:1163-1170, Barkowich,A.J.&Peck,W.W., 1997 Refsum Disease In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987 A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987 Showing articles 0 to 10 of 10