Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/1790
Title: Aqueiropodia : primer reporte de caso en Argentina
Other Titles: Acheiropodia: first case report in Argentina
Authors: Ormazábal, Mariel 
Vaccari, Nelly 
Szulepa, Roberto 
Bidondo, María Paz 
Barbero, Pablo 
Groisman, Boris 
Keywords: Enfermedades en Gemelos;Deformidades Congénitas de la Mano;Deformidades Congénitas del Pie;Recién Nacido
Issue Date: Oct-2015
Project: datasets
Journal: Archivos argentinos de pediatria 
Abstract: 
Acheiropodia is a very rare disease with autosomal recessive inheritance characterized by limb reduction defects. It has been described mainly in Brazil. The aim of this report is to describe the first reported cases in Argentina in two affected twins. Patients were reported to the National Registry of Congenital Anomalies of Argentina (RENAC). Both twins had limb reduction defect including hands, forearms, feet and fibulae. These patients are the first reported cases of acheiropodia syndrome in Argentina. Immigration from Brazil could explain this case in our population.
Description: 
Fil: Ormazabal, Mariel. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.

Fil: Vaccari, Nelly. Hospital SAMIC Oberá, Servicio de Neonatología; Misiones, Argentina.

Fil: Szulepa, Roberto. Hospital SAMIC Oberá, Servicio de Neonatología; Misiones, Argentina.

Fil: Bidondo, María P. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.

Fil: Barbero, Pablo. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.

Fil: Groisman, Boris. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
URI: http://sgc.anlis.gob.ar/handle/123456789/1790
ISSN: 1668-3501
DOI: 10.5546/aap.2015.e299
Rights: Open Access
Creative Commons Attribution 4.0 International License
Appears in Collections:Publicaciones CeNaGeM

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