| Identifier |
wh_ch47_p2536 |
| Title |
Walsh & Hoyt: Autosomal Dominant Ataxias |
| Creator |
Parashkev Nachev, PhD, MRCP(UK); Christopher Kennard, PhD, FRCP, FMed Sci |
| Affiliation |
(PN) University College London; (CK) University of Oxford |
| Subject |
Neurodegenerative Diseases; Metabolic Diseases; Adult; Cerebellar Disorders; Autosomal Dominant Ataxias; Olivopontocerebellar Degeneration |
| Description |
In contrast to the early-onset inherited ataxic disorders, which are predominantly recessive, those with onset after 20 years are usually dominantly inherited. Although there is often little or no spinal involvement, the name spinocerebellar ataxia (SCA) is used generically for the non-episodic dominantly inherited ataxias, and episodic ataxia (EA) for those where the symptoms are intermittent. Autosomal dominant cerebellar ataxia (ADCA). |
| Date |
2005 |
| Language |
eng |
| Format |
application/pdf |
| Type |
Text |
| Source |
Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition |
| Relation is Part of |
Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology |
| Collection |
Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu |
| Publisher |
Wolters Kluwer Health, Philadelphia |
| Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
| Rights Management |
Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
| ARK |
ark:/87278/s6905c9s |
| Setname |
ehsl_novel_whts |
| ID |
186709 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6905c9s |
