Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy

被引:5
作者
Carter, Lauren B. [1 ]
Battaglia, Agatino [2 ]
Cherry, Athena [1 ]
Manning, Melanie A. [1 ]
Ruzhnikov, Maura R. Z. [1 ]
Bird, Lynne M. [3 ,4 ]
Dowsett, Leah [5 ,6 ]
Graham, John M., Jr. [7 ]
Alkuraya, Fowzan S. [8 ]
Hashem, Mais [8 ]
Dinulos, Mary Beth [9 ]
Vallee, Stephanie [9 ]
Adam, Margaret P. [10 ]
Glass, Ian [10 ]
Beck, Anita E. [10 ]
Stevens, Cathy A. [11 ]
Zackai, Elaine [12 ]
McDougall, Carey [12 ]
Keena, Beth [12 ]
Peron, Angela [13 ,14 ]
Vignoli, Aglaia [13 ]
Seaver, Laurie H. [15 ,16 ]
Slavin, Thomas P. [17 ]
Hudgins, Louanne [1 ]
机构
[1] Stanford Univ, Stanford, CA 94305 USA
[2] IRCCS Stella Maris Fdn, Dept Dev Neurosci, Pisa, Italy
[3] Univ Calif San Diego, San Diego, CA 92103 USA
[4] Rady Childrens Hosp San Diego, San Diego, CA USA
[5] Kapiolani Med Ctr, Honolulu, HI USA
[6] Univ Hawaii, Honolulu, HI 96822 USA
[7] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[8] King Faisal Specialist Hosp & Res Ctr, Riyadh, Saudi Arabia
[9] Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA
[10] Univ Washington, Seattle, WA 98195 USA
[11] Univ Tennessee, Sch Med, Knoxville, TN USA
[12] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[13] Univ Milan, San Paolo Hosp, Dept Hlth Sci, Child Neuropsychiat Unit,Epilepsy Ctr, Milan, Italy
[14] Univ Utah, Sch Med, Dept Pediat, Div Med Genet, Salt Lake City, UT USA
[15] Helen DeVos Childrens Hosp, Spectrum Hlth, Grand Rapids, MI USA
[16] Michigan State Univ, Dept Pediat & Human Dev, Grand Rapids, MI USA
[17] City Hope Natl Med Ctr, Div Clin Canc Genom, Duarte, CA USA
关键词
1p36; distress; hypoxic ischemic encephalopathy;
D O I
10.1002/ajmg.a.61266
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:1543 / 1546
页数:4
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