Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome

Pediatric Neurology

Volumn 25, Issue 2, 2001, Pages 166-169

  Hayflick, Susan J ^a,b,h   Penzien, Johann M ^a,c,d   Michl, Wolfgang ^a,d,e   Sharif, Uzma M ^a,f,g   Rosman, N Paul ^a,f,g   Wheeler, Patricia G ^a,f,g  

^a Department of Molecular and Medical Genetics ^*

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c Division of Neuropediatrics

^d Zentralklinikum   (Germany)

^e Division of Pediatric Radiology

^f TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^g TUFTS MEDICAL CENTER   (United States)

^h Mail Code L103a   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IRON;

ACADEMIC ACHIEVEMENT; ADOLESCENT; ADULT; CHILD; CLINICAL ARTICLE; CONFERENCE PAPER; DIAGNOSTIC VALUE; ELECTRORETINOGRAM; FAMILY; FEMALE; HALLERVORDEN SPATZ DISEASE; HUMAN; MALE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOLOGY; PARENT; PRIORITY JOURNAL; SIBLING; SPEECH;

EID: 0034850470     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(01)00296-X     Document Type: Conference Paper

References (7)

1. Hallervorden-Spatz syndrome
2. Hallervorden-Spatz syndrome and brain iron metabolism
3. MR imaging in a case of Hallervorden-Spatz disease
4. MR imaging of a group I case of Hallervorden-Spatz disease
5. Hallervorden-Spatz syndrome; Clinical and magnetic resonance imaging correlations
6. Hallervorden-Spatz disease; Clinical and MRI study of 11 cases diagnosed in life
7. Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13