Characterization of optical coherence topography findings in Kenny-Caffey Syndrome

Journal of AAPOS

Volumn 11, Issue 3, 2007, Pages 291-293

  Timoney, Peter ^a   Darcy, Fiona ^a   McCreery, Kathryn ^b   Reardon, William ^b   Brosnahan, Donal ^a  

^a ROYAL VICTORIA EYE AND EAR HOSPITAL   (Ireland)

^b OUR LADY S CHILDREN S HOSPITAL   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

ACCOMMODATION PARALYSIS; ARTICLE; CASE REPORT; CHILD; CONGENITAL MALFORMATION; GENETIC ANALYSIS; HUMAN; IN SITU HYBRIDIZATION; INTRAOCULAR PRESSURE; KENNY CAFFEY SYNDROME; MALE; MICROGNATHIA; NEWBORN INTENSIVE CARE; OPTICAL COHERENCE TOMOGRAPHY; PAPILLEDEMA; PRIORITY JOURNAL; SHORT STATURE; SYMPTOM; TOPOGRAPHY; TWIN PREGNANCY;

ABNORMALITIES, MULTIPLE; BONE DISEASES, DEVELOPMENTAL; CHILD; DWARFISM; HUMANS; HYPEROPIA; HYPOCALCEMIA; MALE; MICROPHTHALMOS; PAPILLEDEMA; RETINA; RETINAL DISEASES; SYNDROME; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 34250218180     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaapos.2006.09.020     Document Type: Article

References (10)

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9. Majewski F., Rosendahl W., Ranke M., et al. The Kenny syndrome, a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction. Eur J Pediatr 136 (1981) 21-30
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