A clinical case of Zellweger syndrome in a patient with a previous history of ocular medulloepithelioma
Peroxisomal biogenesis disorders (PBDs) are autosomal recessive diseases caused by mutations in one of the 14 PEX genes described in the scientific literature.All of these syndromes may be associated with different mutations in the PEX genes, the most frequent being PEX1 for patients with Zellweger...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2018-07-01
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| Series: | Saudi Journal of Ophthalmology |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1319453417301145 |