Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment—A Case Report

1p36 deletion syndrome represents the most common terminal deletion observed in humans. Major clinical findings comprise developmental delay/intellectual disability, poor or absent expressive language, congenital central muscular hypotonia, brain anomalies, brachydactyly/camptodactyly, short feet, a...

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Detalles Bibliográficos
Autor principal: Briegel, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619815/
https://www.ncbi.nlm.nih.gov/pubmed/34831818
http://dx.doi.org/10.3390/ijerph182212064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619815/
https://www.ncbi.nlm.nih.gov/pubmed/34831818
http://dx.doi.org/10.3390/ijerph182212064

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