HIGHLIGHTS
- who: Caroline Apra1 from the Department of Neurosurgery, Hôpital Necker-Enfants Malades, Paris, France-Centre de référence have published the Article: Changes in FGFR2 amino-acid residue Asn549 lead to Crouzon and Pfeiffer syndrome with hydrocephalus, in the Journal: (JOURNAL)
- what: On a phenotypical point of view, the three patients the authors report present with typical Crouzon or Pfeiffer syndrome: exorbitism, maxillary retrusion, premature suture fusion, and one patient with hand abnormalities.
SUMMARY
Craniosynostosis is a cranial malformation occurring in approximately 1 in 2500 live births. Common variable . . .
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