Developmental prosopagnosia in a patient with hypoplasia of the vermis cerebelli.
نویسندگان
چکیده
; Published online before print May 9, 2012; 2012;78;1700 Neurology J. Van den Stock, M. Vandenbulcke, Q. Zhu, et al. vermis cerebelli Developmental prosopagnosia in a patient with hypoplasia of the July 3, 2013 This information is current as of http://www.neurology.org/content/78/21/1700.full.html located on the World Wide Web at: The online version of this article, along with updated information and services, is Neurology. All rights reserved. Print ISSN: 0028-3878. Online ISSN: 1526-632X. since 1951, it is now a weekly with 48 issues per year. Copyright © 2012 American Academy of ® is the official journal of the American Academy of Neurology. Published continuously Neurology
منابع مشابه
Spasmus nutans and congenital ocular motor apraxia with cerebellar vermian hypoplasia.
BACKGROUND Spasmus nutans and congenital ocular motor apraxia share clinical characteristics. However, their development in a patient with cerebellar vermian hypoplasia has not been previously described. OBJECTIVE To report spasmus nutans and congenital ocular motor apraxia in a child with cerebellar vermian hypoplasia. DESIGN Case report. SETTING Tertiary-care hospital. Patient A 7-year-...
متن کاملسندرم دندی واکر: گزارش یک مورد نادر
Dandy-Walker anomaly is a rare congenital disorder. This syndrome is diagnosed by cerebellar vermis hypoplasia, cystic dilatation of the fourth ventricle and, enlargement of the posterior fossa with or without hydrocephalus. This study presents a report of a male fetus with Dandy-Walker syndrome and determination of clinical protests, risk factors, diagnosis, and treatment of this syndrome. The...
متن کاملNeurocutaneous Melanosis in Association with Dandy-Walker Complex with Extensive Intracerebral and Spinal Cord Involvement
Neurocutaneous melanosis (NCM) is a rare congenital syndrome consisting of benign or malignant melanotic tumors of the central nervous system with large or numerous cutaneous melanocytic nevi. The Dandy-Walker complex (DWC) is characterized by an enlarged posterior fossa with high insertion of the tentorium, hypoplasia or aplasia of the cerebellar vermis, and cystic dilatation of the fourth ven...
متن کاملNovel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia – further expansion of the phenotypic spectrum
BACKGROUND Pontocerebellar hypoplasia type 6 (PCH6) is a mitochondrial disease caused by mutations in the RARS2 gene. RARS2 encodes mitochondrial arginyl transfer RNA synthetase, an enzyme involved in mitochondrial protein translation. A total of 27 patients from 14 families have been reported so far. Characteristic clinical features comprise neonatal lactic acidosis, severe encephalopathy, int...
متن کاملJoubert syndrome: Clinical and radiological characteristics of nine patients
BACKGROUND Joubert Syndrome (JS) is a rare genetic developmental disorder, first identified in 1969. In patients with JS, certain regions of the brain (mainly cerebellar vermis and brainstem) are underdeveloped or malformed. This can lead to impaired attention, visual, spatial, motor, language and social functional skills. JS is characterized by a host of features, many of which do not occur in...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Neurology
دوره 78 21 شماره
صفحات -
تاریخ انتشار 2012