Infantile Hypophosphatasia: Clinical Case
Background. Hypophosphatasia is rare hereditary disease caused by deficiency of the tissue-nonspecific alkaline phosphatase isozyme. It manifests with bone and teeth mineralisation defects, electrolyte imbalance, respiratory disorders, convulsive syndrome, physical developmental delay, nephrocalcino...
Main Authors: | Tatyana V. Gabrusskaya, Yana V. Panutina, Maria O. Revnova, Mikhail M. Kostik |
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Format: | Article |
Language: | English |
Published: |
"Paediatrician" Publishers LLC
2020-02-01
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Series: | Voprosy Sovremennoj Pediatrii |
Subjects: | |
Online Access: | https://vsp.spr-journal.ru/jour/article/view/2259 |
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