Cargando…
Is microcephaly a so-far unrecognized feature of XYY syndrome?()
• 47,XYY syndrome is a frequent sex chromosome aneuploidy. • Overview of characteristic symptoms of 47,XXY; • First report of 47,XYY and microcephaly in a preterm child; • Brief differential diagnosis of microcephaly.
Autores principales: | Nguyen-Minh, Sylvie, Bührer, Christoph, Hübner, Christoph, Kaindl, Angela M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287790/ https://www.ncbi.nlm.nih.gov/pubmed/25606399 http://dx.doi.org/10.1016/j.mgene.2013.10.013 |
Ejemplares similares
-
Large homozygous RAB3GAP1 gene microdeletion causes Warburg Micro Syndrome 1
por: Picker-Minh, Sylvie, et al.
Publicado: (2014) -
Immature Teratoma and Subsequent Acute Promyelocytic Leukemia in a Pediatric Patient With XYY Syndrome
por: Park, Ju-Heon, et al.
Publicado: (2015) -
Adenocarcinoma - success so far and the way ahead
por: Fatima, Rabab, et al.
Publicado: (2023) -
“Precision psychiatry”: A promising direction so far
por: Khanra, Sourav, et al.
Publicado: (2018) -
Coronary artery aneurysms—a truly rare entity or simply unrecognized so far?
por: Nikolaidou, Chrysovalantou N, et al.
Publicado: (2019)