Pillay Syndrome (Ophthalmomandibulomelic Dysplasia) 727f59h 727f59h 727f59h
General: Autosomal dominant; both sexes affected.
Ocular: Corneal opacities.
Clinical: Temporomandibular fusion; obtuse mandibular angle; short forearms.
Magalini SI, Scrascia E. Dictionary of Medical Syndromes. 2nd ed. Philadelphia: Lippincott, 1981.
Pillay VK. Ophthalmomandibulomelic dysplasia. An hereditary syndrome. J Bone Joint Surg 1964; 46:858-862.
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