Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy.
1p36
distress
hypoxic ischemic encephalopathy
Journal
American journal of medical genetics. Part A
ISSN: 1552-4833
Titre abrégé: Am J Med Genet A
Pays: United States
ID NLM: 101235741
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
21
02
2019
revised:
16
05
2019
accepted:
01
06
2019
pubmed:
18
6
2019
medline:
29
7
2020
entrez:
18
6
2019
Statut:
ppublish
Résumé
1p36 deletion syndrome is a well-described condition with a recognizable phenotype, including cognitive impairment, seizures, and structural brain anomalies such as periventricular leukomalacia (PVL). In a large series of these individuals by Battaglia et al., "birth history was notable in 50% of the cases for varying degrees of perinatal distress." Given the potential for perinatal distress, seizures and PVL, we questioned if this disorder has clinical overlap with hypoxic ischemic encephalopathy (HIE). We reviewed the medical records of 69 individuals with 1p36 deletion to clarify the perinatal phenotype of this disorder and determine if there is evidence of perinatal distress and/or hypoxic injury. Our data provides evidence that these babies have signs of perinatal distress. The majority (59% term; 75% preterm) needed resuscitation and approximately 18% had cardiac arrest. Most had abnormal brain imaging (84% term; 73% preterm) with abnormal white matter findings in over half of patients. PVL or suggestion of "hypoxic insult" was present in 18% of term and 45% of preterm patients. In conclusion, individuals with 1p36 deletion have evidence of perinatal distress, white matter changes, and seizures, which can mimic HIE but are likely related to their underlying chromosome disorder.
Identifiants
pubmed: 31207089
doi: 10.1002/ajmg.a.61266
pmc: PMC7254578
mid: NIHMS1574849
doi:
Types de publication
Journal Article
Meta-Analysis
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1543-1546Subventions
Organisme : NCI NIH HHS
ID : K08 CA234394
Pays : United States
Informations de copyright
© 2019 Wiley Periodicals, Inc.
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