Oculomotor apraxia: The presenting sign of Gaucher disease

Pediatric Neurology - Tập 5 - Trang 128-129 - 1989
Varda Gross-Tsur1, Yehuda Har-Even1, Isaac Gutman2, Naomi Amir1
1Neuropediatric Unit; Bikur Cholim Hospital; Jerusalem, Israel.
2Neuroophthalmogical Unit; Tel Hashomer Hospital; Jerusalem, Israel.

Tài liệu tham khảo

Fredrickson, 1983, Glucosylceramide lipidoses: Gaucher disease, 842 Devine, 1982, Chromosomal localization of the gene for Gaucher disease, 511 Miller, 1973, Gaucher's disease: Neurologic disorder in adult siblings, Ann Intern Med, 78, 883, 10.7326/0003-4819-78-6-883 Sanders, 1976, Ocular movements in lipid storage disease: Reports of juvenile Gaucher disease and the ophthalmoplegic lipidosis, Birth Defects, 12, 535 Tripp, 1977, Juvenile Gaucher's disease with horizontal gaze palsy in three siblings, J Neurol Neurosurg Psychiatry, 40, 470, 10.1136/jnnp.40.5.470 Cogan, 1981, Ocular motor signs in some metabolic diseases, Arch Ophthalmol, 99, 1802, 10.1001/archopht.1981.03930020676010 Stowens, 1982, Oculomotor deficits in Gaucher disease, 143 Erikson, 1986, Gaucher disease — Norrbottnian type III, Acta Paediatr Scand, 326, 1, 10.1111/j.1651-2227.1986.tb14936.x