Objectives/hypothesis: To describe spontaneous hearing improvement in the first years of life of a number of preterm neonates relative to cochlear implant candidacy.
Study Design: Retrospective case study.
Methods: Hearing levels of 14 preterm neonates (mean gestational age at birth = 29 weeks) referred after newborn hearing screening were evaluated.
In a cohort of 103 females clinically diagnosed with Rett syndrome (RTT), 91 had a detectable MECP2 mutation. Emphasis on details of natural history facilitated grouping of females with the same MECP2 mutation and the development of so-called disorder profiles. Some examples of disorder profiles of different recurrent MECP2 mutations are discussed.
View Article and Find Full Text PDFInt J Pediatr Otorhinolaryngol
December 2007
Objective: Assessment of the level of psychosocial adaptation in Dutch young school children with persistent and/or recurrent otitis media compared to a U.S. community sample.
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