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Pillay syndrome (ophthalmomandibulomelic dysplasia)


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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