Enzyme Replacement Therapy In Hypophosphatasia
Author(s) -
Seyit Ahmet Uçaktürk,
Selin Elmaoğulları,
Sevim Ünal,
Deniz Gönülal,
Eda Mengen
Publication year - 2018
Publication title -
journal of college of physicians and surgeons pakistan
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.229
H-Index - 33
eISSN - 1681-7168
pISSN - 1022-386X
DOI - 10.29271/jcpsp.2018.09.s198
Subject(s) - hypophosphatasia , enzyme replacement therapy , respiratory distress , alkaline phosphatase , medicine , disease , pediatrics , enzyme , endocrinology , gastroenterology , surgery , chemistry , biochemistry
Hypophosphatasia (HPP) is associated with significant morbidity and mortality in pediatric patients. The disease also imposes a high disease-burden in adult-onset HPP. Asfotase alfa (AA) is the first-in-class, bone-targeted, enzyme- replacement therapy designated to reverse the skeletal mineralisation defects in HPP. A male newborn presented with extreme fontanel gap and respiratory distress. He was diagnosed with perinatal lethal HPP thus AA treatment was started. Serum alkaline phosphatase (ALP) levels increased as high as 12,700 U/L during treatment. Any side effect related to AA was not observed. AA may be a valuable emerging therapy for the treatment of HPP.
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