Pathologic Features of Dilated Cardiomyopathy with Localized Noncompaction in a Child with Deletion 1p36 Syndrome

被引：3

作者：

Pearce, F. Bennett ^{[1
]}

Litovsky, Silvio H. ^{[2
]}

Dabal, Robert J. ^{[3
]}

Robin, Nathaniel ^{[4
]}

Dure, Leon J. ^{[1
]}

George, James F. ^{[3
]}

Kirklin, James K. ^{[3
]}

机构：

[1] Univ Alabama, Sch Med, Dept Pediat, Birmingham, AL USA

[2] Univ Alabama, Sch Med, Dept Pathol, Birmingham, AL USA

[3] Univ Alabama, Sch Med, Dept Surg, Birmingham, AL 35294 USA

[4] Univ Alabama, Sch Med, Dept Clin Genet, Birmingham, AL USA

来源：

CONGENITAL HEART DISEASE | 2012年 / 7卷 / 01期

关键词：

Dilated Cardiomyopathy; Noncompaction; Deletion; 1p36; VENTRICULAR NON-COMPACTION; MONOSOMY; 1P36;

D O I：

10.1111/j.1747-0803.2011.00514.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Dilated cardiomyopathy and ventricular noncompaction have been reported in association with deletion 1p36 syndrome. Previous descriptions include echocardiographic and/or gross pathologic descriptions. There are no previous reports of microscopic findings. We report a case with descriptions of echocardiographic, gross pathologic, and microscopic findings.

引用

页码：59 / 61

页数：3

共 50 条

[31] A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu Syndrome
Tan, TY
Bankier, A
Slater, HR
Northrop, EL
Zacharin, M
Savarirayan, R
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 139A (03) : 216 - 220
[32] Left Ventricular Noncompaction: A Rare Disorder in Adults and Its Association With 1p36 Chromosomal Anomaly
Dod, Harvinder S.
Bhardwaj, Ravindra
Hummel, Marybeth
Morise, Anthony P.
Batish, Satdev
Warden, Bradford E.
Beto, Robert J.
Jain, Abnash C.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (01) : 191 - 195
[33] Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review
Yokoyama, Emiy
Villarroel, Camilo E.
Diaz, Sinhue
Del Castillo, Victoria
Perez-Vera, Patricia
Salas, Consuelo
Gomez, Samuel
Barreda, Renee
Molina, Bertha
Frias, Sara
MOLECULAR CYTOGENETICS, 2020, 13 (01)
[34] Is 1p36 Deletion Associated with Anterior Body Wall Defects?
Collu, Medis
Yuksel, Sirin
Sirin, Basak Kumbasar
Abbasoglu, Latif
Alanay, Yasemin
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (07) : 1889 - 1894
[35] Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36
Lissauer, D.
Larkins, S. A.
Sharif, S.
MacPherson, L.
Rhodes, C.
Kilby, M. D.
PRENATAL DIAGNOSIS, 2007, 27 (09) : 874 - 878
[36] Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report
Nistico, D.
Guidolin, F.
Navarra, C. O.
Bobbo, M.
Magnolato, A.
D'Adamo, A. P.
Giorgio, E.
Pivetta, B.
Barbi, E.
Gasparini, P.
Cadenaro, M.
Sirchia, F.
BMC PEDIATRICS, 2020, 20 (01)
[37] 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients
Jacquin, Clemence
Landais, Emilie
Poirsier, Celine
Afenjar, Alexandra
Akhavi, Ahmad
Bednarek, Nathalie
Benech, Caroline
Bonnard, Adeline
Bosquet, Damien
Burglen, Lydie
Callier, Patrick
Chantot-Bastaraud, Sandra
Coubes, Christine
Coutton, Charles
Delobel, Bruno
Descharmes, Margaux
Dupont, Jean-Michel
Gatinois, Vincent
Gruchy, Nicolas
Guterman, Sarah
Heddar, Abdelkader
Herissant, Lucas
Heron, Delphine
Isidor, Bertrand
Jaeger, Pauline
Jouret, Guillaume
Keren, Boris
Kuentz, Paul
Le Caignec, Cedric
Levy, Jonathan
Lopez, Nathalie
Manssens, Zoe
Martin-Coignard, Dominique
Marey, Isabelle
Mignot, Cyril
Missirian, Chantal
Pebrel-Richard, Celine
Pinson, Lucile
Puechberty, Jacques
Redon, Sylvia
Sanlaville, Damien
Spodenkiewicz, Marta
Tabet, Anne-Claude
Verloes, Alain
Vieville, Gaelle
Yardin, Catherine
Vialard, Francois
Doco-Fenzy, Martine
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (02) : 445 - 458
[38] CHROMOSOME 1P36 DELETION SYNDROME: PRENATAL DIAGNOSIS, MOLECULAR CYTOGENETIC CHARACTERIZATION AND FETAL ULTRASOUND FINDINGS
Chen, Chih-Ping
Chen, Ming
Su, Yi-Ning
Hsu, Chin-Yuan
Tsai, Fuu-Jen
Chern, Schu-Rern
Wu, Pei-Chen
Lee, Chen-Chi
Wan, Wayseen
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2010, 49 (04): : 473 - 480
[39] Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications
Shimada, Shino
Shimojima, Keiko
Okamoto, Nobuhiko
Sangu, Noriko
Hirasawa, Kyoko
Matsuo, Mari
Ikeuchi, Mayo
Shimakawa, Shuichi
Shimizu, Kenji
Mizuno, Seiji
Kubota, Masaya
Adachi, Masao
Saito, Yoshiaki
Tomiwa, Kiyotaka
Haginoya, Kazuhiro
Numabe, Hironao
Kako, Yuko
Hayashi, Ai
Sakamoto, Haruko
Hiraki, Yoko
Minami, Koichi
Takemoto, Kiyoshi
Watanabe, Kyoko
Miura, Kiyokuni
Chiyonobu, Tomohiro
Kumada, Tomohiro
Imai, Katsumi
Maegaki, Yoshihiro
Nagata, Satoru
Kosaki, Kenjiro
Izumi, Tatsuro
Nagai, Toshiro
Yamamoto, Toshiyuki
BRAIN & DEVELOPMENT, 2015, 37 (05) : 515 - 526
[40] Bilateral Perisylvian Polymicrogyria, Periventricular Nodular Heterotopia, and Left Ventricular Noncompaction in a Girl With 10.5-11.1 Mb Terminal Deletion of 1p36
Saito, Shoji
Kawamura, Rie
Kosho, Tomoki
Shimizu, Takashi
Aoyama, Koki
Koike, Kenichi
Wada, Takahito
Matsumoto, Naotnichi
Kato, Mitsuhiro
Wakui, Keiko
Fukushima, Yoshimitsu
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (22) : 2891 - 2897

← 1 2 3 4 5 →