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2019, Number 2

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Rev Clin Esc Med 2019; 9 (2)

HETEROTAXIA: Situs ambiguo, síndrome de Ivermark o síndrome de asplenia-poliesplenia

Madrigal JS, Bonilla AC, Sánchez JE
Full text How to cite this article

Language: Spanish
References: 8
Page: 70-76
PDF size: 435.56 Kb.


Key words:

heterotaxy, situs ambiguos, heart disease.

ABSTRACT

Heterotaxia syndrome is a rare pathology that occurs due to a disruption during the embryonic development of the orientation of the axis, which can lead to multiple alterations in the presence, location and function of thoracoabdominal organs.


REFERENCES

  1. Lowenthal A Tacy T Punn R. Heterotaxy: Anatomy, clinical features, and diagnosis. 2018. 1-35.

  2. Hrusca A Rachisan A Lucian B Oprita S Manole S et al. Ivermark syndrome - a rare entity with specific anatominal features. Rev méd Chile. 2015; 143: 34-35.

  3. Icardo J García J Ros M. Malformaciones cardíacas, heterotaxia y lateralidad. Rev Esp Cardiol. 2002; 55: 962-74.

  4. Brueckner M. Heterotaxia, Congenital Heart Disease, and Primary Ciliary Dyskinesia. Circulation. 2007; 115: 2793–2795.

  5. Choi M Borenstein S Hornberger L Langer J. Heterotaxia syndrome: the role of screening for intestinal rotation abnormalities. Arch Dis Child. 2005; 90: 813–815.

  6. Osorio J. Síndrome de Heterotaxia Visceral asociado a una cardiopatía compleja cianógena de flujo pulmonar aumentado y bloqueo atrioventricular completo: reporte de caso. Elservier. 2013; 1: 1-42.

  7. Abut E Arman A Guvel H et al. Malposition of internal organs: A case of situs ambiguous anomaly in an adult. Turk J Gastroenterol. 2003; 14 (2): 151-155.

  8. Wilhelm A Holbert J. Situs Inversus Imaging. Mayo Clinic. 2018. Medscape




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Rev Clin Esc Med. 2019;9