Cargando…
A novel BBS10 mutation identified in a patient with Bardet–Biedl syndrome with a violent emotional outbreak
We report a 10-year-old girl with Bardet–Biedl syndrome caused by a novel mutation in the Bardet–Biedl syndrome 10 (BBS10) gene. She had multiple malformations, including a dysmorphic face, postaxial polydactyly, polycystic kidney and amblyopia. She presented with typical BBS features, including int...
Autores principales: | Ohto, Tatsuyuki, Enokizono, Takashi, Tanaka, Ryuta, Tanaka, Mai, Suzuki, Hisato, Sakai, Aiko, Imagawa, Kazuo, Fukushima, Hiroko, Fukushima, Takashi, Sumazaki, Ryo, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550758/ https://www.ncbi.nlm.nih.gov/pubmed/28808579 http://dx.doi.org/10.1038/hgv.2017.33 |
Ejemplares similares
-
A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay
por: Ueno, Yuichi, et al.
Publicado: (2019) -
A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2
por: Saeki, Saki, et al.
Publicado: (2019) -
Novel ARX mutation identified in infantile spasm syndrome patient
por: Takeshita, Yohei, et al.
Publicado: (2020) -
Bardet-Biedl Syndrome as a Chaperonopathy: Dissecting the Major Role of Chaperonin-Like BBS Proteins (BBS6-BBS10-BBS12)
por: Álvarez-Satta, María, et al.
Publicado: (2017) -
Mutation profile of BBS genes in patients with Bardet–Biedl syndrome: an Italian study
por: Manara, Elena, et al.
Publicado: (2019)