Literature DB >> 7749436

A syndrome involving immunodeficiency and multiple intestinal atresias.

M E Rothenberg1, F V White, B Chilmonczyk, T Chatila.   

Abstract

Multiple intestinal atresias (MIA) is a severe form of intestinal atresias throughout the gastrointestinal tract. In two reports, MIA have been associated with severe immunodeficiency. We report a newborn girl who had profound humoral and B cell immunodeficiency and impaired T cell function. The patient had agammaglobulinemia and decreased blood lymphocytes, with virtually no B cells in the blood or in intestinal lymph nodes. T cells were reduced in number and weakly proliferated to mitogens. These data suggest that a syndrome involving the development of MIA is associated with various forms of severe immunodeficiency, and therefore newborns with MIA should be examined for immunodeficiency.

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Mesh:

Year:  1995        PMID: 7749436

Source DB:  PubMed          Journal:  Immunodeficiency        ISSN: 1067-795X


  7 in total

Review 1.  Hereditary multiple intestinal atresia (HMIA) with severe combined immunodeficiency (SCID): a case report of two siblings and review of the literature on MIA, HMIA and HMIA with immunodeficiency over the last 50 years.

Authors:  Yasser Ali Hussein Ali; Sajjad Rahman; Venkatraman Bhat; Sheikha Al Thani; Adel Ismail; Ibrahim Bassiouny
Journal:  BMJ Case Rep       Date:  2011-02-09

2.  Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.

Authors:  Rui Chen; Silvia Giliani; Gaetana Lanzi; George I Mias; Silvia Lonardi; Kerry Dobbs; John Manis; Hogune Im; Jennifer E Gallagher; Douglas H Phanstiel; Ghia Euskirchen; Philippe Lacroute; Keith Bettinger; Daniele Moratto; Katja Weinacht; Davide Montin; Eleonora Gallo; Giovanna Mangili; Fulvio Porta; Lucia D Notarangelo; Stefania Pedretti; Waleed Al-Herz; Wasmi Alfahdli; Anne Marie Comeau; Russell S Traister; Sung-Yun Pai; Graziella Carella; Fabio Facchetti; Kari C Nadeau; Michael Snyder; Luigi D Notarangelo
Journal:  J Allergy Clin Immunol       Date:  2013-07-04       Impact factor: 14.290

Review 3.  Lymph node pathology in primary combined immunodeficiency diseases.

Authors:  F Facchetti; L Blanzuoli; M Ungari; O Alebardi; W Vermi
Journal:  Springer Semin Immunopathol       Date:  1998

4.  Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort.

Authors:  Isabel Fernandez; Natalie Patey; Valérie Marchand; Mirela Birlea; Bruno Maranda; Elie Haddad; Hélène Decaluwe; Françoise Le Deist
Journal:  Medicine (Baltimore)       Date:  2014-12       Impact factor: 1.889

5.  Congenital pyloric atresia: a report of two cases.

Authors:  Maaen Tayeb; Suzie Khogeer; Amna Fallatah; Mustafa A Hamchou
Journal:  Ann Saudi Med       Date:  2005 Mar-Apr       Impact factor: 1.526

6.  TTC7A mutations disrupt intestinal epithelial apicobasal polarity.

Authors:  Amélie E Bigorgne; Henner F Farin; Roxane Lemoine; Nizar Mahlaoui; Nathalie Lambert; Marine Gil; Ansgar Schulz; Pierre Philippet; Patrick Schlesser; Tore G Abrahamsen; Knut Oymar; E Graham Davies; Christian Lycke Ellingsen; Emmanuelle Leteurtre; Brigitte Moreau-Massart; Dominique Berrebi; Christine Bole-Feysot; Patrick Nischke; Nicole Brousse; Alain Fischer; Hans Clevers; Geneviève de Saint Basile
Journal:  J Clin Invest       Date:  2014-01       Impact factor: 14.808

7.  Congenital intrinsic duodenal obstruction: a review of 35 cases.

Authors:  Ahmed Hassan Al-Salem
Journal:  Ann Saudi Med       Date:  2007 Jul-Aug       Impact factor: 1.526

  7 in total

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