Maxillofacial manifestations of Proteus syndrome: a systematic review with a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology, Nuclear Medicine and imaging,Dentistry (miscellaneous)
Link
http://link.springer.com/content/pdf/10.1007/s11282-019-00416-y.pdf
Reference28 articles.
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2. Cohen MM. Proteus syndrome review: molecular, clinical, and pathologic features. Clin Genet. 2014;85:111–9.
3. Wiedemann HR, Burgio GR, Aldenhoff P, Kunze J, Kaufmann HJ, Schirg E. The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. Eur J Pediatr. 1983;140:5–12.
4. Lindhurst MJ, Sapp JC, Teer JK, et al. A mosaic activating mutation in AKT1 associated with the Proteus syndrome. N Engl J Med. 2011;365:611–9.
5. Turner JT, Cohen MM, Biesecker LG. Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases. Am J Med Genet. 2004;130A:111–22.
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