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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Bibliografiset tiedot

Päätekijät:	Ja Un Moon, Sook Kyung Yum
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	MDPI AG 2023-08-01
Sarja:	Children
Aiheet:	21q deletion hypoxic-ischemic encephalopathy ring chromosome microdeletion refractory seizure
Linkit:	https://www.mdpi.com/2227-9067/10/9/1461
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