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Dilatation of the ventricular cavity

MedGen UID:
1393082
Concept ID:
C4476545
Anatomical Abnormality
Synonym: Ventricular aneurysm
 
HPO: HP:0006698

Definition

A localized outpouching of ventricular cavity that is generally associated with dyskinesia and paradoxical expansion during systole. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVDilatation of the ventricular cavity

Conditions with this feature

Arrhythmogenic right ventricular dysplasia 9
MedGen UID:
373205
Concept ID:
C1836906
Disease or Syndrome
ARVC may not cause any symptoms in its early stages. However, affected individuals may still be at risk of sudden death, especially during strenuous exercise. When symptoms occur, they most commonly include a sensation of fluttering or pounding in the chest (palpitations), light-headedness, and fainting (syncope). Over time, ARVC can also cause shortness of breath and abnormal swelling in the legs or abdomen. If the myocardium becomes severely damaged in the later stages of the disease, it can lead to heart failure.\n\nArrhythmogenic right ventricular cardiomyopathy (ARVC) is a form of heart disease that usually appears in adulthood. ARVC is a disorder of the myocardium, which is the muscular wall of the heart. This condition causes part of the myocardium to break down over time, increasing the risk of an abnormal heartbeat (arrhythmia) and sudden death.
Atrial standstill 2
MedGen UID:
816731
Concept ID:
C3810401
Disease or Syndrome
Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005). For a discussion of genetic heterogeneity of atrial standstill, see ATRST1 (108770).
Liver disease, severe congenital
MedGen UID:
1823968
Concept ID:
C5774195
Disease or Syndrome
Severe congenital liver disease (SCOLIV) is an autosomal recessive disorder characterized by the onset of progressive hepatic dysfunction usually in the first years of life. Affected individuals show feeding difficulties with failure to thrive and features such as jaundice, hepatomegaly, and abdominal distension. Laboratory workup is consistent with hepatic insufficiency and may also show coagulation defects, anemia, or metabolic disturbances. Cirrhosis and hypernodularity are commonly observed on liver biopsy. Many patients die of liver failure in early childhood (Moreno Traspas et al., 2022).

Professional guidelines

PubMed

Weber EC, Recker F, Herberg U, Oberhoffer R, Kurkevych A, Axt-Fliedner R, Geipel A, Gembruch U, Berg C, Gottschalk I
Ultraschall Med 2023 Aug;44(4):e184-e190. Epub 2022 May 5 doi: 10.1055/a-1823-0821. PMID: 35512837
Gray B, Semsarian C
Clin Cardiol 2020 Aug;43(8):915-920. Epub 2020 Jan 11 doi: 10.1002/clc.23289. PMID: 31925963Free PMC Article
Hutter D, Silverman ED, Jaeggi ET
Scand J Immunol 2010 Sep;72(3):235-41. doi: 10.1111/j.1365-3083.2010.02440.x. PMID: 20696021

Recent clinical studies

Etiology

Dziewięcka E, Winiarczyk M, Wiśniowska-Śmiałek S, Karabinowska-Małocha A, Robak J, Kaciczak M, Baranowski F, Rubiś P
Cardiology 2023;148(5):395-401. Epub 2023 Jun 13 doi: 10.1159/000531534. PMID: 37311443
Weber EC, Recker F, Herberg U, Oberhoffer R, Kurkevych A, Axt-Fliedner R, Geipel A, Gembruch U, Berg C, Gottschalk I
Ultraschall Med 2023 Aug;44(4):e184-e190. Epub 2022 May 5 doi: 10.1055/a-1823-0821. PMID: 35512837
Cabeza JF, Aristizábal-Duque CH, Sánchez IMB, Ortiz MR, Almodóvar AR, Ortega MD, Martínez FE, Saldaña MR, Del Pozo FJF, Álvarez-Ossorio MP, Rubio MDM
Eur J Pediatr 2022 May;181(5):1943-1949. Epub 2022 Jan 25 doi: 10.1007/s00431-022-04384-0. PMID: 35075570
Gray B, Semsarian C
Clin Cardiol 2020 Aug;43(8):915-920. Epub 2020 Jan 11 doi: 10.1002/clc.23289. PMID: 31925963Free PMC Article
Travain MI, Wexler JP
Semin Nucl Med 1999 Oct;29(4):298-318. doi: 10.1016/s0001-2998(99)80018-x. PMID: 10534233

Diagnosis

Dziewięcka E, Winiarczyk M, Wiśniowska-Śmiałek S, Karabinowska-Małocha A, Robak J, Kaciczak M, Baranowski F, Rubiś P
Cardiology 2023;148(5):395-401. Epub 2023 Jun 13 doi: 10.1159/000531534. PMID: 37311443
Weber EC, Recker F, Herberg U, Oberhoffer R, Kurkevych A, Axt-Fliedner R, Geipel A, Gembruch U, Berg C, Gottschalk I
Ultraschall Med 2023 Aug;44(4):e184-e190. Epub 2022 May 5 doi: 10.1055/a-1823-0821. PMID: 35512837
Gray B, Semsarian C
Clin Cardiol 2020 Aug;43(8):915-920. Epub 2020 Jan 11 doi: 10.1002/clc.23289. PMID: 31925963Free PMC Article
Travain MI, Wexler JP
Semin Nucl Med 1999 Oct;29(4):298-318. doi: 10.1016/s0001-2998(99)80018-x. PMID: 10534233
Waller BF
J Am Soc Echocardiogr 1988 Jan-Feb;1(1):4-19. doi: 10.1016/s0894-7317(88)80060-9. PMID: 3078540

Therapy

Yu C, Yue Z, Shi M, Jiang L, Chen S, Yao M, Yu Q, Wu X, Zhang H, Yao F, Wang C, Sun H, Li J
ACS Nano 2022 Oct 25;16(10):16234-16248. Epub 2022 Oct 3 doi: 10.1021/acsnano.2c05168. PMID: 36190461
Lu DY, Yalçin H, Sivalokanathan S, Greenland GV, Vasquez N, Yalçin F, Zhao M, Valenta I, Ganz P, Pampaloni MH, Zimmerman S, Schindler TH, Abraham TP, Abraham MR
J Nucl Cardiol 2020 Dec;27(6):2031-2043. Epub 2018 Nov 19 doi: 10.1007/s12350-018-01521-x. PMID: 30456498
Kawamata H, Kawasaki T, Kamitani T, Yoshioka K, Matoba S, Sugihara H
J Electrocardiol 2018 Sep-Oct;51(5):895-897. Epub 2018 Jun 26 doi: 10.1016/j.jelectrocard.2018.06.014. PMID: 30177336
Hutter D, Silverman ED, Jaeggi ET
Scand J Immunol 2010 Sep;72(3):235-41. doi: 10.1111/j.1365-3083.2010.02440.x. PMID: 20696021
Opie LH, Walpoth B, Barsacchi R
J Mol Cell Cardiol 1985 Jul;17 Suppl 2:21-34. doi: 10.1016/0022-2828(85)90005-7. PMID: 2863385

Prognosis

Dziewięcka E, Winiarczyk M, Wiśniowska-Śmiałek S, Karabinowska-Małocha A, Robak J, Kaciczak M, Baranowski F, Rubiś P
Cardiology 2023;148(5):395-401. Epub 2023 Jun 13 doi: 10.1159/000531534. PMID: 37311443
Weber EC, Recker F, Herberg U, Oberhoffer R, Kurkevych A, Axt-Fliedner R, Geipel A, Gembruch U, Berg C, Gottschalk I
Ultraschall Med 2023 Aug;44(4):e184-e190. Epub 2022 May 5 doi: 10.1055/a-1823-0821. PMID: 35512837
Gray B, Semsarian C
Clin Cardiol 2020 Aug;43(8):915-920. Epub 2020 Jan 11 doi: 10.1002/clc.23289. PMID: 31925963Free PMC Article
Roberts WC, Burks KH, Ko JM, Filardo G, Guileyardo JM
Am J Cardiol 2015 Jan 1;115(1):125-40. Epub 2014 Oct 13 doi: 10.1016/j.amjcard.2014.10.004. PMID: 25456862
Travain MI, Wexler JP
Semin Nucl Med 1999 Oct;29(4):298-318. doi: 10.1016/s0001-2998(99)80018-x. PMID: 10534233

Clinical prediction guides

Achten A, Muller SA, Wijk SS, van der Meer MG, van der Harst P, van Tintelen P, Te Riele AS, van Empel V, Oerlemans MI, Knackstedt C
Ann Med 2024 Dec;56(1):2418965. Epub 2024 Oct 26 doi: 10.1080/07853890.2024.2418965. PMID: 39460551Free PMC Article
Weber EC, Recker F, Herberg U, Oberhoffer R, Kurkevych A, Axt-Fliedner R, Geipel A, Gembruch U, Berg C, Gottschalk I
Ultraschall Med 2023 Aug;44(4):e184-e190. Epub 2022 May 5 doi: 10.1055/a-1823-0821. PMID: 35512837
Zavadovskij KV, Saushkin VV, Varlamova YV, Mishkina AI, Shipulin VV, Lebedev DI, Popov SV
Kardiologiia 2021 Jul 31;61(7):14-21. doi: 10.18087/cardio.2021.7.n1420. PMID: 34397337
Raimondi AJ
Childs Nerv Syst 1994 Jan;10(1):2-12. doi: 10.1007/BF00313578. PMID: 8194058
Pfeffer MA, Braunwald E
Circulation 1990 Apr;81(4):1161-72. doi: 10.1161/01.cir.81.4.1161. PMID: 2138525

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