Mid-Aortic Syndrome in Williams-Beuren Syndrome with an Atypical Small-Sized Deletion of Chromosome 7q11.23 as Arteritis

被引:1
|
作者
Byoun, Jeong Tae [1 ]
Cho, Jae Young [1 ]
Yun, Kyeong Ho [1 ]
Rhee, Sang Jae [1 ]
Yu, Seung Taek [2 ]
Oh, Su Jin [1 ]
机构
[1] Wonkwang Univ Hosp, Dept Cardiol, 895 Muwang Ro, Iksan 54538, South Korea
[2] Wonkwang Univ Hosp, Dept Pediat, Iksan, South Korea
关键词
Hypertension; Aortic diseases; PHENOTYPE;
D O I
10.1536/ihj.20-495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mid-aortic syndrome (MAS) is a rare condition characterized by stenosis of the distal thoracic and/or abdominal aorta. Williams-Beuren syndrome (WBS) is a relatively rare cause of MAS. We report a case of incidentally diagnosed MAS caused by WBS without typical manifestations caused by an atypical small-sized deletion in chromosome 7q11.23, which was initially misdiagnosed as Takayasu arteritis.
引用
收藏
页码:207 / 210
页数:4
相关论文
共 50 条
  • [21] Copy number variants at Williams–Beuren syndrome 7q11.23 region
    Giuseppe Merla
    Nicola Brunetti-Pierri
    Lucia Micale
    Carmela Fusco
    Human Genetics, 2010, 128 : 3 - 26
  • [22] Identification of GTF2IRD 1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23
    Franke, Y
    Peoples, RJ
    Francke, U
    CYTOGENETICS AND CELL GENETICS, 1999, 86 (3-4): : 296 - 304
  • [23] Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23
    Antonell, A
    de Luis, O
    Domingo-Roura, X
    Pérez-Jurado, LA
    GENOME RESEARCH, 2005, 15 (09) : 1179 - 1188
  • [24] Infantile spasms in Williams-Beuren syndrome with typical deletions of the 7q11.23 critical region and a review of the literature
    Samanta, Debopam
    ACTA NEUROLOGICA BELGICA, 2017, 117 (01) : 359 - 362
  • [25] Familial Williams-Beuren syndrome caused by an atypical 7q11.2 deletion
    Bernat, John
    MOLECULAR GENETICS AND METABOLISM, 2021, 132 : S180 - S181
  • [26] Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion
    Claudia Torniero
    Bernardo Dalla Bernardina
    Francesca Novara
    Roberto Cerini
    Clara Bonaglia
    Tiziano Pramparo
    Roberto Ciccone
    Renzo Guerrini
    Orsetta Zuffardi
    European Journal of Human Genetics, 2008, 16 : 880 - 887
  • [27] Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion
    Torniero, Claudia
    Bernardina, Bernardo Dalla
    Novara, Francesca
    Cerini, Roberto
    Bonaglia, Clara
    Pramparo, Tiziano
    Ciccone, Roberto
    Guerrini, Renzo
    Zuffardi, Orsetta
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2008, 16 (08) : 880 - 887
  • [28] Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion
    Gagliardi, C
    Bonaglia, MC
    Selicorni, A
    Borgatti, R
    Giorda, R
    JOURNAL OF MEDICAL GENETICS, 2003, 40 (07) : 526 - 530
  • [29] Exploring evolution in ceboidea (Platyrrhini, primatology) by Williams-Beuren (HSA 7q11.23) chromosome mapping
    Picone, Barbara
    Dumas, Francesca
    Stanyon, Roscoe
    Lannino, Antonella
    Bigoni, Francesca
    Privitera, Orsola
    Sineo, Luca
    FOLIA PRIMATOLOGICA, 2008, 79 (05) : 417 - 427
  • [30] Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome
    Ghaffari, Mahsa
    Birgani, Maryam Tahmasebi
    Kariminejad, Roxana
    Saberi, Alihossein
    ANNALS OF HUMAN GENETICS, 2018, 82 (06) : 469 - 476