Brain Hemorrhages in Jacobsen Syndrome: A Retrospective Review of Six Cases and Clinical Recommendations

被引:10
作者
Grossfeld, Paul [1 ]
机构
[1] UCSD Sch Med, Div Cardiol, Dept Pediat, San Diego, CA USA
关键词
Jacobsen syndrome; Paris-Trousseau syndrome; hemorrhagic stroke; TERMINAL DELETION DISORDER; GENE; IDENTIFICATION; DEFECTS;
D O I
10.1002/ajmg.a.38032
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Jacobsen syndrome is a rare chromosomal disorder caused by distal deletions in the long arm of chromosome 11. All patients with Jacobsen syndrome have Paris-Trousseau syndrome, a bleeding disorder that causes neonatal thrombocytopenia, and persistent platelet dysfunction. Despite that, to date there are no reported cases of hemorrhagic strokes occurring in patients with Jacobsen syndrome. In the last 6 years at least six cases of brain hemorrhages in patients with Jacobsen syndrome have occurred. In this report, we perform a retrospective review of these six cases. The analysis indicates that the etiology of brain hemorrhages in Jacobsen syndrome is likely multifactorial. A likely cause (or causes) was identified in three of the cases, and additional potential risk factors were identified. Based on these findings, clinical recommendations are provided that should aid in the identification of those individuals with Jacobsen syndrome that are at increased risk for brain hemorrhages, and will hopefully decrease the occurrence of this devastating complication in people with Jacobsen syndrome. (C) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:667 / 670
页数:4
相关论文
共 14 条
[1]   Evidence for autism spectrum disorder in Jacobsen syndrome: identification of a candidate gene in distal 11q [J].
Akshoomoff, Natacha ;
Mattson, Sarah N. ;
Grossfeld, Paul D. .
GENETICS IN MEDICINE, 2015, 17 (02) :143-148
[2]   Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome) [J].
Coldren, C. D. ;
Lai, Z. ;
Shragg, P. ;
Rossi, E. ;
Glidewell, S. C. ;
Zuffardi, O. ;
Mattina, T. ;
Ivy, D. D. ;
Curfs, L. M. ;
Mattson, S. N. ;
Riley, E. P. ;
Treier, M. ;
Grossfeld, P. D. .
NEUROGENETICS, 2009, 10 (02) :89-95
[3]   The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency [J].
Dalm, Virgil A. S. H. ;
Driessen, Gertjan J. A. ;
Barendregt, Barbara H. ;
van Hagen, Petrus M. ;
van der Burg, Mirjam .
JOURNAL OF CLINICAL IMMUNOLOGY, 2015, 35 (08) :761-768
[4]  
Favier R, 1993, C R ACAD SCI 3, V316, P608
[5]   Jacobsen syndrome: Advances in our knowledge of phenotype and genotype [J].
Favier, Remi ;
Akshoomoff, Natacha ;
Mattson, Sarah ;
Grossfeld, Paul .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2015, 169 (03) :239-250
[6]   Brain Hemorrhages in Jacobsen Syndrome: A Retrospective Review of Six Cases and Clinical Recommendations [J].
Grossfeld, Paul .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (03) :667-670
[7]   The 11q terminal deletion disorder: A prospective study of 110 cases [J].
Grossfeld, PD ;
Mattina, T ;
Lai, Z ;
Favier, R ;
Jones, KL ;
Cotter, F ;
Jones, C .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 129A (01) :51-61
[8]   (11-21) TRANSLOCATION IN 4 GENERATIONS WITH CHROMOSOME 11 ABNORMALITIES IN OFFSPRING - CLINICAL, CYTOGENETICAL, AND GENE MARKER STUDY [J].
JACOBSEN, P ;
HAUGE, M ;
HENNINGSEN, K ;
HOBOLTH, N ;
MIKKELSEN, M ;
PHILIP, J .
HUMAN HEREDITY, 1973, 23 (06) :568-585
[9]   Jacobsen syndrome [J].
Mattina, Teresa ;
Perrotta, Concetta Simona ;
Grossfeld, Paul .
ORPHANET JOURNAL OF RARE DISEASES, 2009, 4
[10]   PX-RICS-deficient mice mimic autism spectrum disorder in Jacobsen syndrome through impaired GABAA receptor trafficking [J].
Nakamura, Tsutomu ;
Arima-Yoshida, Fumiko ;
Sakaue, Fumika ;
Nasu-Nishimura, Yukiko ;
Takeda, Yasuko ;
Matsuura, Ken ;
Akshoomoff, Natacha ;
Mattson, Sarah N. ;
Grossfeld, Paul D. ;
Manabe, Toshiya ;
Akiyama, Tetsu .
NATURE COMMUNICATIONS, 2016, 7