Silver Syndrome (Congenital Hemihypertrophy)
General: Muscular hypertrophy of one side of face; etiology 949g63j unknown; reported association of this condition with a small deletion in chromosome 13.
Ocular: Caf-au-lait spots of the lid.
Clinical: Broad forehead; small triangular face; inverted V-shaped mouth; genitourinary abnormalities; precocious puberty; medullary sponge kidney; Wilms tumor.
Aita JA. Congenital facial anomalies with neurologic defects. Springfield, IL: Charles C. Thomas, 1969.
Beetz R, et al. Medullary sponge kidneys and unilateral Wilms tumor in a child with Beckwith-Wiedemann syndrome. Eur J Pediatr 1991; 150:489-492.
Wahlstrom J, et al. Silver-like syndrome and a small deletion on chromosome 13. Acta Paediatr 1993; 82:993-996.
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