Hypophosphatasia and cleidocranial dysplasia—a case report and review of the literature: the role of the neurosurgeon

Hypophosphatasia (HPT) and cleidocranial dysplasia (CCD) are rare genetic disorders characterized by both defective ossification and bone mineralization. Patients usually present with craniosynostosis and cranial defects which in many cases require surgical repair. There is only 1 reported case of c...

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Veröffentlicht in:	Child's nervous system 2022-02, Vol.38 (2), p.461-464
Hauptverfasser:	Blionas, Alexandros, Friehs, Gerhard M., Zerris, Vasileios A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report Medicine Medicine & Public Health Neurosciences Neurosurgery
Online-Zugang:	Volltext
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