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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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short stature

RAB18 Deficiency

GM1 Gangliosidosis

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Hurler and Scheie Syndromes (MPS IH, IS, IH/S)

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Osteogenesis Imperfecta

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Neurofibromatosis Type I

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Iris in neurofibromatosis

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Facial growths in neurofibromatosis

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Iris showing Lisch nodules

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Maroteaux-Lamy Syndrome (MPS VI)

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Noonan Syndrome

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Facial view of 63 yo with Noonan syndrome.

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Posterior neck view of female with Noonan syndrome

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Low-set ear and neck webbing in Noonan syndrome

Morquio Syndrome (MPS IVB)

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Morquio Syndrome (MPS IVA)

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Lowe Oculocerebrorenal Syndrome

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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