Oculocerebral syndrome with hypopigmentation
Alternate names[edit | edit source]
Cross syndrome; Kramer syndrome; Oculocerebral hypopigmentation syndrome; Hypopigmentation oculocerebral syndrome Cross type
Definition[edit | edit source]
Oculocerebral hypopigmentation syndrome, Cross type is a rare congenital syndrome characterized by cutaneous and ocular hypopigmentation, various ocular anomalies (e.g. corneal and lens opacity, spastic ectropium, and/or nystagmus), growth deficiency, intellectual deficit and other progressive neurologic anomalies such as spastic tetraplegia, hyperreflexia, and/or athetoid movements. The clinical picture varies among patients and may also include other anomalies such as urinary tract abnormalities, Dandy-Walker malformations, and/or bilateral inguinal hernia.
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NIH genetic and rare disease info[edit source]
Oculocerebral syndrome with hypopigmentation is a rare disease.
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