Your Article Summary
See Latest ArticlesA Novel MECP2 Mutation in a Boy with Neonatal Encephalopathy and Facial Dysmorphism
The Journal of Pediatrics, 07/01/09
Julich K et al. - Methly-CpG-binding protein 2 mutations cause Rett syndrome in females. Here authros report on a male infant with neonatal encephalopathy, myoclonic jerks, and irregular breathing patterns caused by a novel frameshift mutation in the MECP2 gene. In addition he has facial dysmorphisms previously not described in these patients.
Today in Pediatrics...keeping you current
Receive free subspecialty "5-minute updates" via email
Why are some children with early onset of asthma getting better over the years? - Diagnostic failure or salutogenetic factors
International Journal of Medical Sciences , 12/04/09
Prevalence of Sexually Transmitted Infections Among Female Adolescents Aged 14 to 19 in the United States
Pediatrics, 12/04/09
Skin-to-Skin Contact and/or Oral 25% Dextrose for Procedural Pain Relief for Term Newborn Infants
Pediatrics, 12/04/09