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Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy.
Carter, Lauren B; Battaglia, Agatino; Cherry, Athena; Manning, Melanie A; Ruzhnikov, Maura Rz; Bird, Lynne M; Dowsett, Leah; Graham, John M; Alkuraya, Fowzan S; Hashem, Mais; Dinulos, Mary Beth; Vallee, Stephanie; Adam, Margaret P; Glass, Ian; Beck, Anita E; Stevens, Cathy A; Zackai, Elaine; McDougall, Carey; Keena, Beth; Peron, Angela; Vignoli, Aglaia; Seaver, Laurie H; Slavin, Thomas P; Hudgins, Louanne.
Afiliação
  • Carter LB; Stanford University, Stanford, California.
  • Battaglia A; Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, Pisa, Italy.
  • Cherry A; Stanford University, Stanford, California.
  • Manning MA; Stanford University, Stanford, California.
  • Ruzhnikov MR; Stanford University, Stanford, California.
  • Bird LM; University of California San Diego and Rady Children's Hospital San Diego, San Diego, California.
  • Dowsett L; Kapi'olani Medical Center and University of Hawai'i, Honolulu, Hawaii.
  • Graham JM; Cedars-Sinai Medical Center, Los Angeles, California.
  • Alkuraya FS; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hashem M; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Dinulos MB; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Vallee S; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Adam MP; University of Washington, Seattle, Washington.
  • Glass I; University of Washington, Seattle, Washington.
  • Beck AE; University of Washington, Seattle, Washington.
  • Stevens CA; University of Tennessee School of Medicine, Knoxville, Tennessee.
  • Zackai E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • McDougall C; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Keena B; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Peron A; Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Vignoli A; Department of Pediatrics, Division of Medical Genetics, University of Utah School of Medicine, Salt Lake City, Utah.
  • Seaver LH; Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Slavin TP; Spectrum Health Helen DeVos Children's Hospital.
  • Hudgins L; Michigan State University Department of Pediatrics and Human Development, Grand Rapids, Michigan.
Am J Med Genet A ; 179(8): 1543-1546, 2019 08.
Article em En | MEDLINE | ID: mdl-31207089
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Hipóxia-Isquemia Encefálica / Transtornos Cromossômicos / Angústia Psicológica Tipo de estudo: Diagnostic_studies / Systematic_reviews Limite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Hipóxia-Isquemia Encefálica / Transtornos Cromossômicos / Angústia Psicológica Tipo de estudo: Diagnostic_studies / Systematic_reviews Limite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article