Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: ALPL-related autosomal recessive hypophosphatasia
Perinatal lethal hypophosphatasia
A rare, genetic form of hypophosphatasia (HPP) characterized by markedly impaired bone mineralization in utero due to reduced activity of serum alkaline phosphatase (ALP) and causing stillbirth or respiratory failure within days of birth.
This condition has no sub-types.