Literature DB >> 26225594

Pentalogy of Cantrell: Case Report With Review of the Literature.

Amy J Jnah1, Desi M Newberry, Amanda England.   

Abstract

BACKGROUND: Pentalogy of Cantrell is a rare, congenital disorder characterized by lower sternal defects, diaphragmatic defect, pericardial defect, supraumbilical abdominal wall abnormalities, and/or intracardiac defects. The collective defects result from failure of either differentiation or migration of mesenchymal or mesodermal structures during the embryonic phase of development. Mortality of the disease complex is high, and treatment, when appropriate, revolves around surgical correction of the associated defects.
PURPOSE: This article presents a case of pentalogy of Cantrell and examines the literature to report the most current evidence relative to the embryology and pathophysiology. In addition, the methods of pre- and postnatal diagnosis, management, and prognostic indicators are examined. METHODS/SEARCH STRATEGY: Case report was gathered from the medical records and is provided as it occurred. The literature was searched for evidence of best management strategies as well as care implications for families. FINDINGS/
RESULTS: A female newborn was delivered at (Equation is included in full-text article.)weeks' gestation secondary to premature onset of labor. Prenatal ultrasonography identified an abdominal wall defect, diaphragmatic hernia, sternal defect, ventricular septal defect, and open neural tube defect. Examination immediately after delivery confirmed prenatal findings and a diagnosis of pentalogy of Cantrell was assigned. IMPLICATIONS FOR PRACTICE: Patients with the diagnosis of pentalogy of Cantrell should receive antenatal counseling relative to mortality and morbidity risks. An interprofessional approach in the immediate timeframe after delivery facilitates timely diagnostics and offers families prompt confirmation of antenatal findings. IMPLICATIONS FOR RESEARCH: Future research can focus on further elucidating genetic etiologies of pentalogy of Cantrell.

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Year:  2015        PMID: 26225594     DOI: 10.1097/ANC.0000000000000209

Source DB:  PubMed          Journal:  Adv Neonatal Care        ISSN: 1536-0903            Impact factor:   1.968


  5 in total

Review 1.  Craniopagus parasiticus: successful separation of a 28-week preterm newborn from parasite sibling twin bearing lethal congenital anomalies associated to Cantrell's pentad and sirenomelia-case-based review of the literature.

Authors:  Adrian Caceres; Juan Luis Segura-Masis; Ariadnna Caceres-Alan; Francisco Gutierrez-Duran; Justiniano Zamora-Chaves; Juan Luis Segura-Valverde
Journal:  Childs Nerv Syst       Date:  2021-05-01       Impact factor: 1.475

Review 2.  Pentalogy of Cantrell.

Authors:  Adele P Williams; Raoud Marayati; Elizabeth A Beierle
Journal:  Semin Pediatr Surg       Date:  2019-04-09       Impact factor: 2.754

3.  The complete spectrum of pentalogy of Cantrell in one of a set of dizygotic twins: A case report of a rare congenital anomaly.

Authors:  Zlatan Zvizdic; Irmina Sefic-Pasic; Amira Mesic; Sabina Terzic; Semir Vranic
Journal:  Medicine (Baltimore)       Date:  2021-04-09       Impact factor: 1.817

4.  NAD+ deficiency in human congenital malformations and miscarriage: A new model of pleiotropy.

Authors:  Paul R Mark
Journal:  Am J Med Genet A       Date:  2022-04-29       Impact factor: 2.578

5.  Abrogation of TGF-beta signalling in TAGLN expressing cells recapitulates Pentalogy of Cantrell in the mouse.

Authors:  Bashar Aldeiri; Urmas Roostalu; Alessandra Albertini; Julia Behnsen; Jason Wong; Antonino Morabito; Giulio Cossu
Journal:  Sci Rep       Date:  2018-02-26       Impact factor: 4.379

  5 in total

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