Literature DB >> 2240032

Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family.

L A Moreno1, F Gottrand, D Turck, S Manouvrier-Hanu, F Mazingue, C Morisot, F Le Deist, C Ricour, C Nihoul-Feketé, P Debeugny.   

Abstract

Hereditary multiple atresias involving the gastrointestinal tract from pylorus to rectum are the most unusual form of intestinal atresia; the type of inheritance was suggested to be autosomal recessive. The inheritance of the severe combined immunodeficiency syndrome can be autosomal recessive or X-linked. We report on 3 sibs with multiple-level intestinal atresias. One sib had severe combined immunodeficiency syndrome and clinical histories of the other 2 sibs strongly suggested a congenital immunodeficiency syndrome. The parents of those children were healthy and nonconsanguineous. To our knowledge, this is the first report of the association of multiple gastrointestinal atresias and immunodeficiency which appears to have an autosomal recessive pattern of transmission. Our family report suggests that, in the presence of multiple gastrointestinal atresias, attention should be given to possible associated immunological disorders.

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Year:  1990        PMID: 2240032     DOI: 10.1002/ajmg.1320370133

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  11 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.  Hereditary Multiple Gastrointestinal Atresia associated with Choledochal Cyst: A Rare Entity with Management Dilemma.

Authors:  Raj P; Sinha Sk; Ramji S; Sarin Yk
Journal:  J Neonatal Surg       Date:  2014-07-10

5.  The complex surgical management of the first case of severe combined immunodeficiency and multiple intestinal atresias surviving after the fourth year of life.

Authors:  Riccardo Guanà; Salvatore Garofano; Elisabetta Teruzzi; Simona Vinardi; Giulia Carbonaro; Alessia Cerrina; Isabella Morra; Davide Montin; Alessandro Mussa; Jürgen Schleef
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

6.  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

Review 7.  Congenital intestinal atresias with multiple episodes of sepsis: A case report and review of literature.

Authors:  Natalia Mandiá; Alejandro Pérez-Muñuzuri; Olalla López-Suárez; Carolina López-Sanguos; Adolfo Bautista-Casanovas; Mariá-Luz Couce
Journal:  Medicine (Baltimore)       Date:  2018-06       Impact factor: 1.889

8.  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

9.  Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.

Authors:  Mark E Samuels; Jacek Majewski; Najmeh Alirezaie; Isabel Fernandez; Ferran Casals; Natalie Patey; Hélène Decaluwe; Isabelle Gosselin; Elie Haddad; Alan Hodgkinson; Youssef Idaghdour; Valerie Marchand; Jacques L Michaud; Marc-André Rodrigue; Sylvie Desjardins; Stéphane Dubois; Francoise Le Deist; Philip Awadalla; Vincent Raymond; Bruno Maranda
Journal:  J Med Genet       Date:  2013-02-19       Impact factor: 6.318

10.  Congenital pyloric atresia and associated anomalies.

Authors:  Ahmed H Al-Salem
Journal:  Pediatr Surg Int       Date:  2007-03-28       Impact factor: 2.003

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