Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/10579
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Type: Journal article
Title: Pfeiffer syndrome: a clinical review.
Author: Moore, M.
Cantrell, S.
Trott, J.
David, D.
Citation: Cleft Palate Craniofacial Journal, 1995; 32(1):62-70
Publisher: American Cleft Palate-Craniofacial Association
Issue Date: 1995
ISSN: 1055-6656
1545-1569
Abstract: The combination of bicoronal craniosynostosis, broad thumbs and great toes, and partial variable soft tissue syndactyly of the hands and feet (i.e., Pfeiffer syndrome) classically followed a benign clinical course. A review of the clinical features of those Pfeiffer syndrome patients presenting to our unit confirm another subgroup in whom the craniofacial and associated manifestations are more extreme, with a significant risk of early demise. The early aggressive surgical management of craniostenosis, hydrocephalus, exorbitism, faciostenosis, and upper airway obstruction has provided the potential for prolonged useful survival in these cases.
Keywords: Skull; Facial Bones; Orbit; Cerebral Ventricles; Humans; Acrocephalosyndactylia; Airway Obstruction; Eye Abnormalities; Treatment Outcome; Follow-Up Studies; Adult; Child; Infant; Infant, Newborn; Female; Male
RMID: 0030004525
DOI: 10.1597/1545-1569(1995)032<0062:PSACR>2.3.CO;2
Appears in Collections:Surgery publications

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