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Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2 by Deconte, Desirée, Kreusch, Tulia Cristina, Salvaro, Bruna Pavan, Perin, Wagner Fernando, Ferreira, Maria Angélica Tosi, Kopacek, Cristiane, da Rosa, Ernani Bohrer, Heringer, Jane Iândora, Ligabue-Braun, Rodrigo, Zen, Paulo Ricardo Gazzola, Rosa, Rafael Fabiano Machado, Fiegenbaum, Marilu

Published in Journal of pediatric genetics (Birmingham, Ala.) (01-12-2020)
“…Abstract Kenny-Caffey syndrome (KCS) is a rare genetic condition characterized by growth retardation, bone abnormalities, and hypoparathyroidism. Herein, we…”

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Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2 by Deconte, Desirée, Kreusch, Tulia Cristina, Salvaro, Bruna Pavan, Perin, Wagner Fernando, Ferreira, Maria Angélica Tosi, Kopacek, Cristiane, da Rosa, Ernani Bohrer, Heringer, Jane Iândora, Ligabue-Braun, Rodrigo, Zen, Paulo Ricardo Gazzola, Rosa, Rafael Fabiano Machado, Fiegenbaum, Marilu

Published in Journal of pediatric genetics (01-12-2020)

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