Postnatal Pancraniosynostosis in a Patient With Infantile Hypophosphatasia

作者:Nahabet Edward H*; Gatherwright James; Vockley Jerry; Henderson Nadene; Tomei Krystal L; Grigorian Adriana P; Kaminski Beth; Bass Nancy; Selman Warren R; Lakin Gregory E
来源:Cleft Palate-Craniofacial Journal, 2016, 53(6): 741-744.
DOI:10.1597/15-027

摘要

Hypophosphatasia is a rare metabolic bone disorder that predisposes patients to craniosynostosis. Typically, patients born with hypophosphatasia will exhibit fused cranial sutures at birth. This is the first reported case of delayed onset of pancraniosynostosis in a patient with infantile hypophosphatasia. The severity of onset and delayed presentation in this patient are of interest and should give pause to those care providers who treat and evaluate patients with hypophosphatasia.

  • 出版日期2016-11