Abstract
Two patients with the Costello syndrome are presented. One was a 7-year-old girl with a history of infantile hypotonia and feeding difficulties. The other was a 3 5/12-year-old boy with a history of neonatal sepsis and respiratory problems. Both had relative macrocephaly at birth, curly hair, large ear lobes, epicanthic folds, a low nasal bridge, thick lips, a short and wide nose, a short neck, a barrel chest, redundant skin, tight Achilles tendons, and pes equinovarus. Nasal papillomata, as described in Costello's two patients, were absent in both patients. Borochowitz et al. (1992) described five patients with what we interpreted as the Costello syndrome but without nasal papillomata. In view of these findings, nasal papillomata are not likely to be essential in the diagnosis of the Costello syndrome. © 1993 The Japan Society of Human Genetics.
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Yoshida, R., Fukushima, Y., Ohashi, H., Asoh, M., & Fukuyama, Y. (1993). The Costello syndrome: Are nasal papillomata essential? The Japanese Journal of Human Genetics, 38(4), 437–444. https://doi.org/10.1007/BF01907992
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