Adult Onset of the Dandy-Walker Syndrome
- 1 October 1978
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 35 (10) , 672-674
- https://doi.org/10.1001/archneur.1978.00500340048009
Abstract
• Two patients with the Dandy-Walker malformation first developed neurologic symptoms in adult life. In both patients there was normal motor and intellectual development during childhood, but as adults they had gradual evolution of brain stem and cerebellar signs and obstructive hydrocephalus. Following resection of the fourth ventricular cyst, both patients recovered. A review of the literature disclosed seven additional patients in whom the Dandy-Walker syndrome was first diagnosed in adult life. These cases illustrate that this congenital brain malformation may not only first become symptomatic later in life, but that it is possible for patients to remain asymptomatic.This publication has 6 references indexed in Scilit:
- The Dandy‐Walker syndromeNeurology, 1972
- THE DANDY-WALKER SYNDROMEJournal of Neuropathology and Experimental Neurology, 1963
- Hydrocephalus SyndromeAmerican Journal of Diseases of Children, 1962
- CONGENITAL HYDROCEPHALUS WITH DEFECTIVE DEVELOPMENT OF THE CEREBELLAR VERMIS (DANDY-WALKER SYNDROME): Clinical and Anatomical Findings in Two Cases with Particular Reference to the So-called Atresia of the Foramina of Magendie and LuschkaJournal of Neurology, Neurosurgery & Psychiatry, 1959
- The Dandy-Walker Syndrome or The So-Called Atresia of the Foramen Magendie*Journal of Neuropathology and Experimental Neurology, 1954
- Congenital Atresia of the Foramina of Luschka and MagendieJournal of Neurosurgery, 1948