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RISS 인기검색어
- 검색키워드
- 저자 : Eduardo A. Perez (검색결과 3 건)
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Marginal Spatialities and Rhizomatic Identifications: Kathy Acker's Discursive Transgressions
Eduardo Barros Grela,Marí,a Bobadilla-Perez 한국아메리카학회 2013 美國學論集 Vol.45 No.1
Deleuze articulation of the concept of rhizome is taken by cultural theory as a collective mechanism of enunciation. With his contribution, he favored the construction of a solid ground for marginal voices acting as legitimate discourses. Also, his discussions of space (later retaken by specialists of the theories of space) problematized traditional epistemological relations that supported a hegemony-resistance pattern whose identity was determined by the existence of oppressed and minority groups. However, as Homi Bhabha claimed, those marginal groups possessed a subversive political agency, and they found in rhizomatic structures a perfect vehicle for the reappropriation (or rather reterritorialization) of space. This article studies the discursive deformations of Kathy Acker's narrative to embody the celebration of those silenced voices, as well as the marginal uprising favored by the postmodern fragmentation of identities. Rooting from Deleuze's principle of multiplicity, Acker's narratives question the relation of multiplicity with subject and subjectivity, and reconcile the performative function of those voices with intertextuality as a machinery of discursive production. Acker uses voice and taboo to resignify conventional hegemonic relations from a political imposture of transgression, violence, and-textual and ethical-decontextualized plagiarism. The deconstructive process necessary to carry out these practices provides several tools of theoretical articulation. Among them, both voice and taboo hold a fundamental position in this essay as they are conceptualized as instruments to problematize marginalization, and consequently, to become aporetic references of postmodern spatialities.
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Waardenburg Syndrome Type IV De Novo SOX10 Variant Causing Chronic Intestinal Pseudo-Obstruction
Anthony R. Hogan,Krishnamurti A. Rao,Willa L. Thorson,Holly L. Neville,Juan E. Sola,Eduardo A. Perez 대한소아소화기영양학회 2019 Pediatric gastroenterology, hepatology & nutrition Vol.22 No.5
Waardenburg syndrome (WS) type IV is characterized by pigmentary abnormalities, deafness and Hirschsprung's disease. This syndrome can be triggered by dysregulation of the SOX10 gene, which belongs to the SOX (SRY-related high-mobility group-box) family of genes. We discuss the first known case of a SOX10 frameshift mutation variant defined as c.895delC causing WS type IV without Hirschsprung's disease. This female patient of unrelated Kuwaiti parents, who tested negative for cystic fibrosis and Hirschsprung's disease, was born with meconium ileus and malrotation and had multiple surgical complications likely due to chronic intestinal pseudo-obstruction. These complications included small intestinal necrosis requiring resection, development of a spontaneous fistula between the duodenum and jejunum after being left in discontinuity, and short gut syndrome. This case and previously reported cases demonstrate that SOX10 gene sequencing is a consideration in WS patients without aganglionosis but with intestinal dysfunction.
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Waardenburg Syndrome Type IV De Novo SOX10 Variant Causing Chronic Intestinal Pseudo-Obstruction
Hogan, Anthony R.,Rao, Krishnamurti A.,Thorson, Willa L.,Neville, Holly L.,Sola, Juan E.,Perez, Eduardo A. The Korean Society of Pediatric Gastroenterology 2019 Pediatric gastroenterology, hepatology & nutrition Vol.22 No.5
Waardenburg syndrome (WS) type IV is characterized by pigmentary abnormalities, deafness and Hirschsprung's disease. This syndrome can be triggered by dysregulation of the SOX10 gene, which belongs to the SOX (SRY-related high-mobility group-box) family of genes. We discuss the first known case of a SOX10 frameshift mutation variant defined as c.895delC causing WS type IV without Hirschsprung's disease. This female patient of unrelated Kuwaiti parents, who tested negative for cystic fibrosis and Hirschsprung's disease, was born with meconium ileus and malrotation and had multiple surgical complications likely due to chronic intestinal pseudo-obstruction. These complications included small intestinal necrosis requiring resection, development of a spontaneous fistula between the duodenum and jejunum after being left in discontinuity, and short gut syndrome. This case and previously reported cases demonstrate that SOX10 gene sequencing is a consideration in WS patients without aganglionosis but with intestinal dysfunction.
KCI
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