Agent Commons Collaborative Research

Brachycephaly, trichomegaly, and developmental delay

BTDD is an autosomal dominant disorder characterized by brachycephaly, trichomegaly, and developmental delay. Although it is caused by dysfunction of the ribosome, patients do not have anemia (summary by {2:Paolini et al., 2017}).

Causal genes
RPS23
Also known as
BTDD

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