Cerebrofacial-Reno-Arthro-Syndactylia Syndrome& 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; & 818b17i nbsp; 225
General: Cause familial?
Ocular: Trichiasis; slanted and asymmetrical size of lid fissure; blepharitis; contraction of visual fields; peripheral pigmentary anomalies of the retina.
Clinical: Mild oligophrenia; small head for body size; slight facial asymmetry; webbed digits; atrophic unilateral sternocleidomastoid muscle; spontaneous shoulder dislocation; small kidneys with renal dysplasia; chronic interstitial nephritis.
Geeraets WJ. Ocular Syndromes. 3rd ed. Philadelphia: Lea & Febiger, 1976.
Greig DM. Hypertelorism: a hitherto undifferentiated congenital craniofacial deformity. Edinburgh Med J 1924; 31:560.
Hanley FJ. Congenital partial hemihypertrophy of the face. J Oral Surg
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