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Congenital Hypophosphatasia


Frank Pessler

, MD, PhD, Helmholtz Centre for Infection Research

Last full review/revision Oct 2020| Content last modified Oct 2020
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Congenital hypophosphatasia is absence or low levels of serum alkaline phosphatase due to mutations in the gene encoding tissue-nonspecific alkaline phosphatase (TNSALP).

Because serum alkaline phosphatase is absent or decreased, calcium is not diffusely deposited in bones, causing low bone density and hypercalcemia Hypercalcemia Hypercalcemia is a total serum calcium concentration > 10.4 mg/dL (> 2.60 mmol/L) or ionized serum calcium > 5.2 mg/dL (> 1.30 mmol/L). Principal causes include hyperparathyroidism, vitamin... read more . Alkaline phosphatase deficiency also causes intracellular pyridoxine deficiency ( vitamin B6 deficiency Vitamin B6 Deficiency and Dependency Because vitamin B6 is present in most foods, dietary deficiency is rare. Secondary deficiency may result from various conditions. Symptoms can include peripheral neuropathy, a pellagra-like... read more ), which can cause generalized seizures. Vomiting, inability to gain weight, and enlargement of the epiphyses (similar to that in rickets) usually occur. Patients who survive infancy have bony deformities and short stature, but mental development is normal.

Asfotase alfa, a recombinant protein carrying the catalytic domain of tissue-nonspecific alkaline phosphatase, can be given by subcutaneous injection for treatment of congenital hypophosphatasia. Dosing is 2 mg/kg 3 times a week or 1 mg/kg 6 times a week; if needed, dose can be increased to 3 mg/kg 3 times a week in children with disease beginning perinatally or during infancy. Vitamin B6 in high doses may reduce seizures; 50 to 100 mg IV is given once for an active seizure, followed by 50 to 100 mg orally once a day. Nonsteroidal anti-inflammatory drugs (NSAIDs) reduce bone pain. Infusions of alkaline phosphatase and bone marrow transplantation have limited roles.

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