Perinatal distress in 1p36 deletion syndrome can mimic 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
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

1543-1546

Subventions

Organisme : NCI NIH HHS
ID : K08 CA234394
Pays : United States

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Lauren B Carter (LB)

Stanford University, Stanford, California.

Agatino Battaglia (A)

Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, Pisa, Italy.

Athena Cherry (A)

Stanford University, Stanford, California.

Melanie A Manning (MA)

Stanford University, Stanford, California.

Maura Rz Ruzhnikov (MR)

Stanford University, Stanford, California.

Lynne M Bird (LM)

University of California San Diego and Rady Children's Hospital San Diego, San Diego, California.

Leah Dowsett (L)

Kapi'olani Medical Center and University of Hawai'i, Honolulu, Hawaii.

John M Graham (JM)

Cedars-Sinai Medical Center, Los Angeles, California.

Fowzan S Alkuraya (FS)

King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Mais Hashem (M)

King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Mary Beth Dinulos (MB)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Stephanie Vallee (S)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Margaret P Adam (MP)

University of Washington, Seattle, Washington.

Ian Glass (I)

University of Washington, Seattle, Washington.

Anita E Beck (AE)

University of Washington, Seattle, Washington.

Cathy A Stevens (CA)

University of Tennessee School of Medicine, Knoxville, Tennessee.

Elaine Zackai (E)

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Carey McDougall (C)

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Beth Keena (B)

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Angela Peron (A)

Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Department of Pediatrics, Division of Medical Genetics, University of Utah School of Medicine, Salt Lake City, Utah.

Aglaia Vignoli (A)

Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

Laurie H Seaver (LH)

Spectrum Health Helen DeVos Children's Hospital.
Michigan State University Department of Pediatrics and Human Development, Grand Rapids, Michigan.

Thomas P Slavin (TP)

Division of Clinical Cancer Genomics, City of Hope, Duarte, California.

Louanne Hudgins (L)

Stanford University, Stanford, California.

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Classifications MeSH