Synonym(s)
HistoryThis section has been translated automatically.
Cross HE et al. 1967
DefinitionThis section has been translated automatically.
Rare, autosomal recessive inherited syndrome (genetic defect not yet clarified) with oculocutaneous hypopigmentation, microphthalmia, corneal opacity, nystagmus, weakness, spasticity (Cross HE et al. 1967). The disease is observed in the Amish.
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ManifestationThis section has been translated automatically.
Skin and eye changes from birth, neurological disorders in the first weeks of life.
TherapyThis section has been translated automatically.
Primarily neurological and ophthalmological clinical picture.
Dermatological: light protection (e.g. Anthelios), eye protection, because of the sensitivity of the skin regular check for malignant transformations.
LiteratureThis section has been translated automatically.
Cross HE et al (1967) A new oculocerebral syndrome with hypopigmentation. J. Pediat. 70: 398-406
- Scheinfeld NS (2003) Syndromic albinism: a review of genetics and phenotypes. Dermatol Online J 9:5.
Recommended articles
Incoming links (3)
Cross-mckusick-breen syndrome; Kramer syndrome; Oculo-cerebral syndrome with hypopigmentation;Outgoing links (1)
Light protection;Disclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
Prof. Dr. med. Peter Altmeyer