Benign paroxysmal tonic upgaze of childhood in a hypotonic infant with Beckwith-Wiedemann syndrome

Clinical and Experimental Ophthalmology

Volumn 36, Issue 3, 2008, Pages 291-292

  Skalicky, Simon E ^a,b   Billson, Frank A ^a,b  

^a UNIVERSITY OF SYDNEY   (Australia)

^b ROYAL PRINCE ALFRED HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; SOMATOMEDIN B;

BECKWITH WIEDEMANN SYNDROME; BENIGN PAROXYSMAL TONIC UPGAZE; CASE REPORT; CLINICAL FEATURE; DISEASE DURATION; DISOMY; EYE DISEASE; FEEDING DISORDER; HUMAN; HYPOGLYCEMIA; INFANT; LETTER; MALE; MUSCLE HYPOTONIA; OXYGEN SATURATION; POLYCYTHEMIA; POSITIVE END EXPIRATORY PRESSURE; RESPIRATORY DISTRESS;

BECKWITH-WIEDEMANN SYNDROME; FIXATION, OCULAR; HUMANS; INFANT; MALE; MUSCLE HYPOTONIA; OCULAR MOTILITY DISORDERS;

EID: 42449123662     PISSN: 14426404     EISSN: 14429071     Source Type: Journal    
DOI: 10.1111/j.1442-9071.2008.01709.x     Document Type: Letter

References (5)

1. Ouvrier RA, Billson F. Benign paroxysmal tonic upgaze of childhood. J Child Neurol 1988; 3: 177-80.
2. Ouvrier RA, Billson F. Paroxysmal tonic upgaze of childhood - a review. Brain Dev 2005; 27: 185-8.
3. Bentov I, Werner H. IGF, IGF receptor and overgrowth syndromes. Pediatr Endocrinol Rev 2004; 1: 352-60.
4. Spalice A, Parisi P, Iannetti P. Paroxysmal tonic upgaze: physiopathological considerations in three additional cases. J Child Neurol 2000; 15: 15-18.
5. Joseph K, Avallone J, Difazio M. Paroxysmal tonic upgaze and partial tetrasomy of chromosome 15: A novel genetic association. J Child Neurol 2005; 20: 165-8.