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Popliteal pterygium syndrome: an orthopaedic perspective.
Oppenheim WL, Larson KR, McNabb MB, Smith CF, Setoguchi Y. Oppenheim WL, et al. J Pediatr Orthop. 1990 Jan-Feb;10(1):58-64. J Pediatr Orthop. 1990. PMID: 2405020 Review.
Popliteal pterygium syndrome (PPS) is a rare autosomal dominant disorder consisting of popliteal webs and craniofacial, genitourinary, and extremity anomalies. ...
Popliteal pterygium syndrome (PPS) is a rare autosomal dominant disorder consisting of popliteal webs and
Periderm: Life-cycle and function during orofacial and epidermal development.
Hammond NL, Dixon J, Dixon MJ. Hammond NL, et al. Semin Cell Dev Biol. 2019 Jul;91:75-83. doi: 10.1016/j.semcdb.2017.08.021. Epub 2017 Aug 10. Semin Cell Dev Biol. 2019. PMID: 28803895 Review.
Disruption of periderm formation and/or function underlies a series of birth defects that exhibit multiple inter-epithelial adhesions including the autosomal dominant popliteal pterygium syndrome and the autosomal recessive cocoon syndrom …
Disruption of periderm formation and/or function underlies a series of birth defects that exhibit multiple inter-epithelial adhesions includ …
A familial case of popliteal pterygium syndrome.
Bertelè G, Mercanti M, Gangini GN, Carletti V. Bertelè G, et al. Minerva Stomatol. 2008 Jun;57(6):309-22. Minerva Stomatol. 2008. PMID: 18617879 Review. English, Italian.
Popliteal pterygium syndrome (PPS) is a rare malformation disorder characterized by autosomal dominant inheritance, highly variable expressivity and incomplete penetrance. The disorder is caused by the mutation of the IRF6 gene and the respectiv
Popliteal pterygium syndrome (PPS) is a rare malformation disorder characterized by autosomal dominant in