Differential (Click to cross reference) alopecia alpha-fetoprotein apraxia of eye movements arrhythmia, cardiac ataxia ataxia telangiectasia ataxia, cerebellar ataxia, truncal automatic implantable cardioverter-defibrillator basal ganglia, calcification of brain atrophy cachexia calcification, intracranial carcinoembryonic antigen carcinoma cardiomyopathy CAT scan, abnormal cataracts cerebellar ataxia, children cerebellar ataxia, hereditary cerebellar atrophy, secondary cerebellar degeneration cerebrovascular accident cerebrovascular accident, young adult children chorea choreoathetosis chromosomal abnormality chromosome 11 chromosome 8 cisterna magna, enlarged Cockayne's syndrome conduction block congestive heart failure developmental retardation diabetes mellitus differential diagnosis drooling dysarthria dysmorphic dystonia ejection fraction ejection fraction, abnormal electroencephalogram electroencephalogram, abnormalities of Emery-Dreifuss muscular dystrophy evoked potentials eye movement, disorders of facial appearance, abnormal familial gene gene mutation genetic diagnosis genetic linkage genetic neurologic disorders gray hair growth retardation hair, loss heart block hyperpigmentation of skin hypogonadism hypotonia immunodeficiency immunosuppression laminopathies leukemia leuko-araiosis LMNA gene lymphoma mental retardation microcephaly misdiagnosis molecular genetics mortality movement disorder movement disorder, extrapyramidal MRI MRI, abnormal multiple system atrophy muscular dystrophy muscular dystrophy, congenital muscular dystrophy, limb-girdle nerve biopsy neurocutaneous disease neuroendocrinology neurologic complications of, systemic disease neurologic disease, diagnoses of neuropathology neuropathy ocular motility, disorders of P300 pacemaker, cardiac-transvenous paraparesis paraparesis, spastic pathology photosensitivity, skin pigmentary retinopathy progeria prognosis radiation hypersensitivity rash review article short stature skin, lesions in neurologic disorders small vessel disease somatosensory evoked potentials spinal muscular atrophy sudden death syncope telangiectases walking, difficulty with Werner's syndrome wheelchair

Showing articles 0 to 6 of 6 The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification Neurol 87:e56-e57, Saini, A.G.,et al, 2016 A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke Neurol 78:e113-e114, Seixas,J.C.,et al, 2012 LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011 Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy Neurol 43:1252-1254, Umehara,F.,et al, 1993 Accelerated Aging of the Brain in Werner's Syndrome Neurol 42:922-924, Kakigi,R.,et al, 1992 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Showing articles 0 to 6 of 6