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Syndrome in question. Costello syndrome
Isy Lima Peixoto1, Ana Maria Carreno1, Vania Mesquita Gadelha Prazeres1
1Amazonas Federal University, Manaus, AM, Brazil.
Abstract:
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects. There is an increased risk of malignancies in these patients, due to the proto-oncogene mutation, and also sudden death secondary to heart disease. We report a case with characteristic phenotype, highlighting the peculiar skin changes.
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