Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
2.
Arch Pediatr ; 15(9): 1498-502, 2008 Sep.
Article in French | MEDLINE | ID: mdl-18674889

ABSTRACT

Wiedemann-Beckwith syndrome (WBS) is a syndrome of excessive growing with a high predisposition to developing embryologic tumours within the first years of life. This risk is evaluated between 7.5 and 10%; it varies with the mechanisms of mutations involved. These take place in two distinct domains of 11p15, which are under parental printing. Emerging techniques of cytogenetic and molecular biology now have shown correlations between genotypes and phenotypes, and can identify the 30% of WBS who are especially at risk of developing tumours. A specific follow-up, integrating the specificity of developing tumours of each 11p15 mutations involved, is now proposed to patients with WBS.


Subject(s)
Beckwith-Wiedemann Syndrome/genetics , Genetic Predisposition to Disease , Neoplasms/genetics , Genotype , Humans , Infant , Phenotype , Risk
3.
Arch Pediatr ; 14(9): 1132-6, 2007 Sep.
Article in French | MEDLINE | ID: mdl-17566719

ABSTRACT

Hepatitis B virus (HBV) is responsible for a worldwide mortality of 1 million people each year. It constitutes a major public health problem, especially in highly endemic zones, where it concerns the youngest children, primarily by a mother to child transmission, with a strong risk of chronic hepatitis infection and hepatocellular carcinoma. Immunisation of children versus HBV is known to be efficient and safe. In Mayotte, a French overseas territory in Indian Ocean, immunisation versus HBV has been introduced since 1993 in the vaccine schedule, starting at day 1 of life. We report hereby the local experience and practice on HBV infection, state of vaccine coverage, and difficulties met with this major public health issue.


Subject(s)
Hepatitis B Vaccines , Hepatitis B/prevention & control , Adult , Clinical Protocols , Comoros/epidemiology , Disease Transmission, Infectious , Female , Hepatitis B/immunology , Hepatitis B/transmission , Hepatitis B, Chronic/epidemiology , Humans , Immunization Schedule , Infant, Newborn , Infectious Disease Transmission, Vertical , Pregnancy , Vaccination/statistics & numerical data
4.
Arch Pediatr ; 14(3): 270-2, 2007 Mar.
Article in French | MEDLINE | ID: mdl-17223023

ABSTRACT

Nontuberculous mycobacterial infections are rare in immunocompetent children, and usually present as adenitis. We report a case of a 6-year-old girl with a multifocal chronic osteomyelitis and pulmonary localisation due to Mycobacterium intracellulare associated with an autosomal dominant mutation of interferon gamma receptor 1 gene (INFGR1) leading to a syndrome of mendelian predisposition to mycobacteria infections by partial deficiency of intracellular signalisation of gamma interferon. This child has been cured with anti-mycobacteria drugs and gamma interferon. This report focus on the importance of looking for a susceptibility of the host to infectious diseases, which can lead to a specific treatment. As far as we know, this is the first case described in a tropical area.


Subject(s)
Mycobacterium avium-intracellulare Infection/diagnosis , Receptors, Interferon/deficiency , Child , Female , France , Humans , Lung Diseases/microbiology , Mutation , Mycobacterium avium-intracellulare Infection/etiology , Osteomyelitis/complications , Osteomyelitis/microbiology , Receptors, Interferon/genetics , Respiratory Tract Infections/complications , Tropical Medicine , Interferon gamma Receptor
SELECTION OF CITATIONS
SEARCH DETAIL