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Novel Nonsense Mutation in ASXL3 causing Bainbridge-Ropers Syndrome
Lingyan Qiao1, Yusheng Liu2, Juan Ge3
1Medical Department, Qingdao University and Department of Pediatric Endocrinology and Genetic Metabolic Diseases, Qingdao Women and Children's Hospital, Qingdao, China.
Background:
Bainbridge-Ropers syndrome is a rare autosomal dominant genetic disorder.
Case Characteristics:
A 26-day-old neonate presented with feeding difficulties, excessive sleeping, and hirsutism over forehead and lumbosacral skin.
Outcome:
Whole-exome sequencing identified a novel nonsense mutation.
Message:
We report a novel mutation in a Chinese neonate with Bainbridge-Ropers syndrome.
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