Hypophosphatasia in a newborn infant
Infantile type hypophosphatasia, an autosomal recessive disease with severe clinical manifestations, is characterized biochemically by subnormal activities of circulating alkaline phosphatase. In this report, we presented a five-day-old male with this rare disorder. His parents were first cou...
| Published in: | The Turkish Journal of Pediatrics |
|---|---|
| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Hacettepe University Institute of Child Health
1995-01-01
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| Online Access: | https://turkjpediatr.org/article/view/3540 |