Cargando…
The Diagnostic Significance of Comorbidities of Congenital Heart Diseases, Low-Set Ears, and Intrauterine Growth Restriction in Neonates With Trisomies 13 and 18
BACKGROUND: Trisomies 13 and 18 (T13/18) are autosomal trisomy syndromes with dismal prognoses. Deciding whether to perform a chromosomal analysis for the definitive diagnosis is often difficult (even for experienced pediatricians) because representative clinical signs may not be found in all T13/18...
Autores principales: | Fujii, Yoshimitsu, Kanda, Eriko, Hirabayashi, Masato, Mine, Kenji, Ohashi, Atsushi, Tsuji, Shoji, Kaneko, Kazunari |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045559/ https://www.ncbi.nlm.nih.gov/pubmed/27713807 http://dx.doi.org/10.5812/ijp.3783 |
Ejemplares similares
-
B-type natriuretic peptide for assessment of haemodynamically significant patent ductus arteriosus in premature infants
por: Mine, Kenji, et al.
Publicado: (2013) -
Intrauterine Growth Retardation Fetus with Trisomy 16 Mosaicism
por: Chareonsirisuthigul, Takol, et al.
Publicado: (2014) -
Association of Neonatal Jaundice with Gut Dysbiosis Characterized by Decreased Bifidobacteriales
por: Akagawa, Shohei, et al.
Publicado: (2021) -
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study
por: Puccio, Giuseppe, et al.
Publicado: (2013) -
IGF1 gene is epigenetically activated in preterm infants with intrauterine growth restriction
por: Kantake, Masato, et al.
Publicado: (2020)