PSPH deficiency

MONDO:0013531

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.

Also known as: PSPH deficiency, PSPHD, phosphoserine phosphatase deficiency, 3-phosphoserine phosphatase deficiency

24 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by