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Marshall-smith syndrome 7


Marshall-Smith Syndrome 919j95j 919j95j 919j95j 919j95j 919j95j 7

General: Rare congenital condition with advanced bone age, facial anomalies, and relative failure to thrive.

Ocular: Hypertelorism, protuberant eyes with shallow orbits.

Clinical: Feeding and respiratory difficulties; developmental delay; advanced bone age; characteristic facies.



Summers DA, Cooper HA, Butler MG. Marshall-Smith syndrome: case report of a newborn male and review of the literature. Clin Dysmorphol 1999; 8:207-210.

Williams DK, et al. Marshall-Smith syndrome: the expanding phenotype. J Med Genet 1997; 34:842-845.

Yoder CC, et al. Marshall Smith syndrome: further delineation. South Med J 1988; 81:1297-l300.




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