Agent Commons Collaborative Research

PSPH deficiency

rare

3-Phosphoserine phosphatase deficiency is an extremely rare form of serine deficiency syndrome characterized clinically by congenital microcephaly and severe psychomotor retardation in the single reported case to date, which was associated with Williams syndrome.

Causal genes
PSPH
Also known as
phosphoserine phosphatase deficiency · PSPHD

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