Negative ERGs in mucopolysaccharidoses (MPS) Hurler–Scheie (I-H/S) and Hurler (I-H)-syndromes

Author:

Tzetzi D.,Hamilton R.,Robinson P. H.,Dutton G. N.

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Sensory Systems,Ophthalmology

Reference22 articles.

1. Kliegman RM, Muenzer JL (2004) Mucopolysaccharidoses. In: Behram RE, Kliegman RM, Jenson HB (eds) Nelson textbook of pediatrics. W.B. Saunders Company Philadelphia, pp 482–486

2. Taylor D (1997) Neurometabolic disease. In: Taylor D (ed) Paediatric ophthalmology. Blackwell Science Ltd Oxford, pp 772–793

3. Jensen OA, Pedersen C, Vestermark S, Warburg M (1980) The Hurler/Scheie phenotype in children from a consanguineous marriage: case report with electronmicroscopy of the conjunctiva and ERG. Metab Pediatr Ophthalmol 4:133–134

4. Caruso RC, Kaiser-Kupfer MI, Muenzer J, Ludwig IH, Zasloff MA, Mercer PA (1986) Electroretinographic findings in the mucopolysaccharidoses. Ophthalmology 93:1612–1616

5. Gullingsrud EO, Krivit W, Summers CG (1998) Ocular abnormalities in the mucopolysaccharidoses after bone marrow transplantation. Ophthalmology 105:1099–1105

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