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KIFF11 Mutation: A Boy with Painless, Progressive Vision Loss, and Nyctalopia
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KIFF11 Mutation: A Boy with Painless, Progressive Vision Loss, and Nyctalopia

Maja Kostic and Carlos Mendoza-Santiesteban
Fundamentals of Pediatric Neuro-Ophthalmology: a Practical, Case-Based Approach to Diagnosis and Management, pp.271-274
2023-01-01

Abstract

And mental retardation (MCLMR) Autosomal dominant microcephaly with chorioretinopathy Chorioretinal dysplasia KIF11 Lymphedema Mental retardation Microcephaly Nyctalopia Progressive vision loss

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