Incidental Radiologic Findings in the 22q11.2 Deletion Syndrome
نویسندگان
چکیده
منابع مشابه
Incidental Radiologic Findings in the 22q11.2 Deletion Syndrome
BACKGROUND AND PURPOSE The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that results in cognitive delays and an increased risk of several psychiatric disorders, particularly schizophrenia. The current study investigates the prevalence of incidental neuroradiologic findings within this population and their relationships with psychiatric conditions. MATERIALS AND METHODS...
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Departments of Pediatrics, Laboratory Medicine, Orofacial Sciences, Program in Craniofacial and Mesenchymal Biology and Institute for Human Genetics, University of California San Francisco, San Francisco, California, USA Correspondence to Ophir D. Klein, MD, PhD, Department of Pediatrics, University of California San Francisco, 513 Parnassus Ave, HSE1509, San Francisco, CA 94143, USA Tel: + 1 4...
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BACKGROUND AND PURPOSE This paper describes the CT findings that characterize the middle and inner ear anomalies in coloboma, heart defects, choanal atresia, mental retardation, genitourinary, and ear anomalies (CHARGE) syndrome. With this information, neuroradiologists will be better prepared to provide clinically relevant information to their referring physicians regarding this rare syndrome....
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ژورنال
عنوان ژورنال: American Journal of Neuroradiology
سال: 2014
ISSN: 0195-6108,1936-959X
DOI: 10.3174/ajnr.a4003