Search Results - "Heringer, Jane Iândora"
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Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2
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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