Infantile Hypophosphatasia: Transplantation Therapy Trial Using Bone Fragments and Cultured Osteoblasts

Background: Hypophosphatasia (HPP) is a rare, heritable, metabolic bone disease due to deficient activity of the tissue-nonspecific isoenzyme of alkaline phosphatase. The infantile form features severe rickets often causing death in the first year of life from respiratory complications. There is no...

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Veröffentlicht in:	The journal of clinical endocrinology and metabolism 2007-08, Vol.92 (8), p.2923-2930
Hauptverfasser:	Cahill, Richard A., Wenkert, Deborah, Perlman, Sharon A., Steele, Ann, Coburn, Stephen P., McAlister, William H., Mumm, Steven, Whyte, Michael P.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alkaline Phosphatase - blood Alkaline Phosphatase - genetics Biological and medical sciences Bone Marrow Transplantation Bone Transplantation Cell Differentiation - physiology Cell Proliferation Cells, Cultured Child Cytogenetics DNA - genetics Endocrinopathies Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology Humans Hypercalcemia - etiology Hypophosphatasia - complications Hypophosphatasia - therapy Infant Knee - diagnostic imaging Medical sciences Osteoblasts - transplantation Radiography Reverse Transcriptase Polymerase Chain Reaction Stem Cells - physiology Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology
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