Cargando…
11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report
BACKGROUND: 11q23 deletion syndrome, also known as Jacobsen syndrome, is characterized by growth retardation, psychomotor retardation, facial dysmorphism, multiple congenital abnormalities, and thrombocytopenia. In 11q23 deletion syndrome, it is often difficult to anticipate the severity of bleeding...
Autores principales: | Ichimiya, Yuko, Wada, Yuka, Kunishima, Shinji, Tsukamoto, Keiko, Kosaki, Rika, Sago, Haruhiko, Ishiguro, Akira, Ito, Yushi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757304/ https://www.ncbi.nlm.nih.gov/pubmed/29307309 http://dx.doi.org/10.1186/s13256-017-1535-5 |
Ejemplares similares
-
Jacobsen syndrome
por: Mattina, Teresa, et al.
Publicado: (2009) -
The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency
por: Dalm, Virgil A. S. H., et al.
Publicado: (2015) -
Trisomy 9 Mosaicism Diagnosed In Utero
por: Takahashi, Hironori, et al.
Publicado: (2010) -
Jacobsen syndrome and neonatal bleeding: report on two unrelated patients
por: Serra, Gregorio, et al.
Publicado: (2021) -
Partial deletion of distal long arm encompassing Jacobsen Syndrome
por: Desai, Manisha, et al.
Publicado: (2014)