Cardiac MRI Characteristics of Noonan Syndrome Associated With Hypertrophic Cardiomyopathy and Congenital Heart Disease

被引：0
|
作者：
Peng, Zhengxuan [1 ]
Ma, Xiaoyan [1 ]
Li, Shibo [1 ]
Liu, Xingguang [2 ]
Zhou, Xing [3 ]
机构：
[1] Gansu Univ Chinese Med, Clin Med Coll 1, Lanzhou, Peoples R China
[2] Gansu Prov Hosp, Dept Cardiovasc Surg, Lanzhou, Peoples R China
[3] Gansu Prov Hosp, Dept Radiol, 204 Donggang West Rd, Lanzhou 730000, Gansu, Peoples R China
来源：
KOREAN JOURNAL OF RADIOLOGY | 2025年 / 26卷 / 04期
关键词：
Noonan syndrome; Special facial features; Myocardial hypertrophy; Gene variant;
D O I：
10.3348/kjr.2024.1316
中图分类号：
R8 [特种医学]; R445 [影像诊断学];
学科分类号：
1002 ; 100207 ; 1009 ;
摘要：
引用
收藏
页码：394 / 396
页数：3
相关论文
共 50 条
  • [21] RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndrome
    Zheng, Jingjing
    Peng, Longyun
    Cheng, Ruofei
    Li, Zhiyan
    Xie, Jianjie
    Huang, Erwen
    Cheng, Jianding
    Zhao, Qianhao
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2024, 12 (01):
  • [22] UNUSUAL COMBINATION OF CONGENITAL HEART-DEFECTS IN AN INFANT WITH NOONAN SYNDROME
    FEIT, LR
    HANSEN, K
    OYER, CE
    WERNER, JC
    PEDIATRIC CARDIOLOGY, 1995, 16 (02) : 95 - 99
  • [23] Double-chambered right ventricle complicated by hypertrophic obstructive cardiomyopathy diagnosed as Noonan syndrome
    Yamamoto, Masahiro
    Takashio, Seiji
    Nakashima, Naoya
    Hanatani, Shinsuke
    Arima, Yuichiro
    Sakamoto, Kenji
    Yamamoto, Eiichiro
    Kaikita, Koichi
    Aoki, Yoko
    Tsujita, Kenichi
    ESC HEART FAILURE, 2020, 7 (02): : 721 - 726
  • [24] Proptosis secondary to bilateral extraocular muscle enlargement in Noonan syndrome with hypertrophic cardiomyopathy: A case report
    Marchione, Giulia
    Pilotto, Elisabetta
    Midena, Giulia
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2023, 33 (05) : NP67 - NP70
  • [25] Noonan syndrome or new autosomal dominant condition with coaretation of the aorta, hypertrophic cardiomyopathy, and minor anomalies
    Lemire, EG
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 113 (03): : 286 - 290
  • [26] Congenital heart defects in Noonan syndrome and PTPN11 muta□onCongenital heart defects in Noonan syndrome and PTPN11 mutation
    Popa, Laura Claudia
    Andreescu, Nicoleta
    Farcas, Simona
    Chirita-Emandi, Adela
    Puiu, Maria
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 185 - 186
  • [27] Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant
    Carvalho, DR
    Alves, VVB
    Minaré-Junior, A
    Peres, LC
    Pina-Neto, JM
    Ramos, ES
    CLINICAL DYSMORPHOLOGY, 2003, 12 (02) : 143 - 144
  • [28] A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy
    Kunihiko Takahashi
    Shigetoyo Kogaki
    Shunji Kurotobi
    Sayaka Nasuno
    Makiko Ohta
    Hitomi Okabe
    Kazuko Wada
    Norio Sakai
    Masako Taniike
    Keiichi Ozono
    European Journal of Pediatrics, 2005, 164 : 497 - 500
  • [29] Atypical, severe hypertrophic cardiomyopathy in a newborn presenting Noonan syndrome harboring a recurrent heterozygous MRAS variant
    Pires, Lucas Vieira Lacerda
    Bordim, Renata de Almeida
    Maciel, Maria Beatriz Rabelo
    Tanaka, Ana Cristina Sayuri
    Yamamoto, Guilherme Lopes
    Honjo, Rachel Sayuri
    Kim, Chong Ae
    Bertola, Debora Romeo
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (10) : 3099 - 3103
  • [30] General anesthesia with remimazolam for tooth extraction in a patient with Noonan syndrome and hypertrophic obstructive cardiomyopathy: A case report
    Kamio, Hisanobu
    Oue, Kana
    Asada, Yasuyuki
    Ito, Nanako
    Imamura, Serika
    Doi, Mitsuru
    Shimizu, Yoshitaka
    Yoshida, Mitsuhiro
    Yanamoto, Souichi
    Hanamoto, Hiroshi
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY, 2025, 37 (01) : 108 - 111
12345