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Congenital anomalies of the immune system: newborn screening, early intervention, genetic counseling and epidemiological study

Grant number: 12/51233-2
Support type:Research Grants - Research in Public Policies for the National Health Care System (PP-SUS)
Duration: July 01, 2013 - June 30, 2015
Field of knowledge:Health Sciences - Medicine
Cooperation agreement: CNPq - PPSUS
Principal Investigator:Antonio Condino Neto
Grantee:Antonio Condino Neto
Home Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
Associated grant(s):14/50291-4 - Early diagnosis of primary immunodeficiencies associated with B/T lymphopenia, AP.R

Abstract

Primary immunodeficiency disorders (PIDD) are congenital disorders leading to high susceptibility to severe and recurrent infections with early onset, high morbidity and mortality, and elevated social and economic cost for the health systems. This project aims the implementation of newborn screening tests and early diagnosis of primary immunodeficiencies, specifically T cell lymphopenias like Di George syndrome (DGS), estimated to be the most common genetic deletion syndrome (1:3000 live births) and Severe Combined Immunodeficiency (SCID), a group of diseases with diverse genetic causes, with a fatal outcome up to 2 years of life unless diagnosed and properly treated. The methodology, TRECs measuring using real time PCR, already available in our laboratory is the gold standard method, has proved successful and is under current use in 7 states in the USA, Japan and some European countries, with promising results. International Registries of Primary Immunodeficiencies indicate that a high number of undiagnosed patients will be accounted , and treated correctly after implementation of molecular detection techniques by means of the newborn screening for PID, reducing morbidity and mortality. Moreover, their families will be supported and will receive genetic counseling. Ali this will be possible in the public health system, once our project will be developed in an SUS (Sistema Único de Saúde) accredited service. (AU)

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
MARILIA PYLES P. KANEGAE; LUCILA AKUNE BARREIROS; JUSLEY LIRA SOUSA; MARCO ANTÔNIO S. BRITO; EDGAR BORGES DE OLIVEIRA JUNIOR; LARA PEREIRA SOARES; JULIANA THEMUDO L. MAZZUCCHELLI; DÉBORA QUIORATO FERNANDES; SONIA MARCHEZI HADACHI; SILVIA MAIA HOLANDA; FLAVIA ALICE T. M. GUIMARÃES; MAURA APARECIDA P. V. V. BOACNIN; MARLEY APARECIDA L. PEREIRA; JOAQUINA MARIA C. BUENO; ANETE SEVCIOVIC GRUMACH; REGINA SUMIKO W. DI GESU; AMÉLIA MIYASHIRO N. DOS SANTOS; NEWTON BELLESI; BEATRIZ T. COSTA-CARVALHO; ANTONIO CONDINO-NETO. TRIAGEM NEONATAL DE IMUNODEFICIÊNCIAS GRAVES COMBINADAS POR MEIO DE TRECS E KRECS: SEGUNDO ESTUDO PILOTO NO BRASIL. Revista Paulista de Pediatria, v. 35, n. 1, p. 25-32, Mar. 2017.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.