Mimicking Hypoxic-Ischemic Encephalopathy in a Newborn with 21q Deletion Originating from Ring Chromosome 21

Partial deletion of the long arm (q) in chromosome 21 is an extremely rare condition with various phenotypes, including microcephaly, neurodevelopmental delay, dysmorphic features, and epileptic seizures. Neonatal hypoxic-ischemic encephalopathy (HIE) is an encephalopathy associated with a hypoxic-i...

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Detalles Bibliográficos
Autores principales: Moon, Ja Un, Yum, Sook Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529320/
https://www.ncbi.nlm.nih.gov/pubmed/37761422
http://dx.doi.org/10.3390/children10091461

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529320/
https://www.ncbi.nlm.nih.gov/pubmed/37761422
http://dx.doi.org/10.3390/children10091461

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