A novel BBS10 mutation identified in a patient with Bardet-Biedl syndrome with a violent emotional outbreak.
Hum Genome Var
; 4: 17033, 2017.
Article
em En
| MEDLINE
| ID: mdl-28808579
ABSTRACT
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 intellectual disability with emotional outbursts and mild obesity. Whole-exome sequencing identified compound heterozygous mutations with NM_024685.3c.1677C>A [p.(Tyr559*)] and c.1974T>G [p.(Tyr658*)]. To our knowledge, the latter mutation has never been reported previously.
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MEDLINE
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Ano de publicação:
2017
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Article