Novel membrane frizzled‐related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds |
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Authors: | Rosemarie A Wasmann Jolien S Klein Wassink‐Ruiter Olof H Sundin Elisa Morales Joke B G M Verheij Jan Willem R Pott |
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Institution: | 1. Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands;2. Department of Clinical Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands;3. Department of Biomedical Sciences Center of Excellence for Neuroscience, Foster School of Medicine, Texas Tech Health Sciences Center, El Paso, Texas, USA |
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Abstract: | Purpose: We present a genetic and clinical analysis of two sisters, 3 and 4 years of age, with nanophthalmos and macular folds. Methods: Ophthalmological examination, general paediatric examination and molecular genetic analysis of the MFRP gene were performed in both affected siblings. Results: Clinical analysis showed high hyperopia (+11 D and +12 D), short axial lengths (15 mm) and the presence of macular folds and optic nerve head drusen. Autofluorescence of the retina was generally normal with subtle macular abnormalities. Sequence analysis showed compound heterozygosity for severe MFRP mutations in both sisters: a previously reported p.Asn167fs (c.498dupC) and a novel stop codon mutation p.Gln91X (c.271C>T). Conclusion: These are the youngest nanophthalmos patients in the literature identified with severe loss of MFRP function, showing already the known structural abnormalities for this disease. Adult patients affected by homozygous or compound heterozygous MFRP mutations generally show signs of retinal dystrophy, with ERG disturbances and RPE abnormalities on autofluorescence imaging. ERG examination could not be performed in these children, but extensive RPE abnormalities were not seen at this young age. |
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Keywords: | hyperopia macular folds membrane frizzled‐related protein gene MFRP nanophthalmos |
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