Article
Schizophreniform presentation and abrupt neurologic decline in a patient with late-onset mucopolysaccharidosis type IIIB.
Psychiatric genetics - 1 Oct 2021
Montenegro Yorran Hardman Araújo, Baldo Guilherme, Giugliani Roberto, Poswar Fabiano de Oliveira, Sobrinho Ruy Pires de Oliveira, Steiner Carlos Eduardo
Abstract excerpt
Due to their low frequency and some atypical presentations, inborn errors of metabolism are frequently misdiagnosed or underdiagnosed, which hinders the correct management of these patients. To illustrate that, here we present a patient that, at early school age, had learning disabilities compared to her classmates, especially for writing. She completed basic education in a regular school and was transferred to a...
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