Blatt Syndrome (Cranio-Orbito-Ocular Dysraphia) 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 737g61h 152
General: Autosomal dominant; characterized by distichiasis and anisometropia; both sexes affected; present from birth.
Ocular: Hypertelorism; microphthalmos; distichiasis with the meibomian glands usually absent; anisometropia.
Clinical: Meningocele or meningoencephalocele; cranial deformities; malformations of facial bones.
Blatt N. Cranio-orbito-ocular dysraphia and meningocele. Rev Otoneuroophthalmol 1961; 33:185.
Duke-Elder S, ed. System of Ophthalmology, vol. III, part 2. St. Louis: CV Mosby, 1976.
Magalini SI, Scrascia E. Dictionary of Medical Syndromes, 2nd ed. Philadelphia: JB Lippincott, 1981.
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