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Quoted phrase not found in phrase index: "Hallux varus-preaxial polysyndactyly syndrome"
Page 1
Forefoot malformations, deformities and other congenital defects in children.
Rampal V, Giuliano F. Rampal V, et al. Orthop Traumatol Surg Res. 2020 Feb;106(1S):S115-S123. doi: 10.1016/j.otsr.2019.03.021. Epub 2019 Oct 21. Orthop Traumatol Surg Res. 2020. PMID: 31648997 Free article. Review.
Congenital pathologies of the forefoot encompass two broad entities with vastly different treatments and prognosis: malformations, which occur during the embryonic period and cause anatomical defects, and deformations, which occur during the fetal period on a foot that is …
Congenital pathologies of the forefoot encompass two broad entities with vastly different treatments and prognosis: malformations, wh …
Minimally Invasive Hallux Interphalangeal Joint Arthrodesis for Hallux Varus in Pfeiffer Syndrome: A Case Report.
Flora M, Diniz P, Neto AL, Teixeira N, Carvalho P, Pinto FG. Flora M, et al. J Foot Ankle Surg. 2018 Jan-Feb;57(1):205-209. doi: 10.1053/j.jfas.2017.08.003. Epub 2017 Nov 3. J Foot Ankle Surg. 2018. PMID: 29103889
It is one of the acrocephalosyndactyly diseases causing cranial malformations owing to early suture fusion. In the foot, it is typically associated with hallux varus, first ray hyperplasia, and partial lesser digit syndactyly. We report a clinical case of a 10-year- …
It is one of the acrocephalosyndactyly diseases causing cranial malformations owing to early suture fusion. In the foot, it is typically ass …
Problems in polydactyly of the foot.
Venn-Watson EA. Venn-Watson EA. Orthop Clin North Am. 1976 Oct;7(4):909-27. Orthop Clin North Am. 1976. PMID: 185565
Polydactyly associated with a short first metatarsal and congenital hallux varus carriers a poorer treatment prognosis and may require continuing treatment. 8. ...
Polydactyly associated with a short first metatarsal and congenital hallux varus carriers a poorer treatment prognosis and may …
The pattern of skeletal anomalies in the cervical spine, hands and feet in patients with Saethre-Chotzen syndrome and Muenke-type mutation.
Trusen A, Beissert M, Collmann H, Darge K. Trusen A, et al. Pediatr Radiol. 2003 Mar;33(3):168-72. doi: 10.1007/s00247-002-0823-3. Epub 2002 Nov 12. Pediatr Radiol. 2003. PMID: 12612814
BACKGROUND: Saethre-Chotzen syndrome (SCS) and Muenke-type mutation (MTM) are complex syndromes with craniosynostosis and skeletal anomalies including syndactyly, carpal and tarsal fusions, and cervical spine abnormalities. ...Duplicated distal phalanx of the hal …
BACKGROUND: Saethre-Chotzen syndrome (SCS) and Muenke-type mutation (MTM) are complex syndromes with craniosynostosis and skeletal an …
Craniosynostosis: Acrocephalosyndactyly (Apert Syndrome) Diagnosed in a Newborn.
Stomnaroska O, Danilovski D, Ivanovska S. Stomnaroska O, et al. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Dec 1;38(3):153-155. doi: 10.2478/prilozi-2018-0016. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017. PMID: 29668474 Free article.
Distal phalanges of the thumbs were broad as well as distal hallux. There was cutaneous syndactyly of the feet. Mental development at the age of 11 months was normal. Apert syndrome is a sporadic disorder. Rarely, inheritance is autosomal dominant. ...
Distal phalanges of the thumbs were broad as well as distal hallux. There was cutaneous syndactyly of the feet. Mental develop …
Mohr-Claussen syndrome or oro-facial-digital syndrome (OFDS) type-II.
Biswas A, Ghosh JK, Sinha MK, Basu K, Chatterjee S. Biswas A, et al. J Pak Med Assoc. 2009 Jul;59(7):484-6. J Pak Med Assoc. 2009. PMID: 19579742
The Mohr-Claussen syndrome or oro-facial-digital syndrome type II (OFD-II)] is characterised by tongue lobulation, midline cleft lip, high arched or cleft palate, broad nasal root with wide bifid nasal tip, hypertelorism, micrognathia, brachydactyly, syndactyly …
The Mohr-Claussen syndrome or oro-facial-digital syndrome type II (OFD-II)] is characterised by tongue lobulation, midline cle …
Malleolus externus plasty for joint reconstruction in fibular aplasia: preliminary report of a new technique.
Weber M, Siebert CH, Goost H, Johannisson R, Wirtz D. Weber M, et al. J Pediatr Orthop B. 2002 Jul;11(3):265-73. doi: 10.1097/00009957-200207000-00013. J Pediatr Orthop B. 2002. PMID: 12089506
Furthermore, he showed a tibial antecurvation deformity of 20 degrees, a fourth ray foot with adduction deformity of the hindfoot, cutane syndactyly D 2-4, and a hallux varus. This new technique works on the following principle. ...
Furthermore, he showed a tibial antecurvation deformity of 20 degrees, a fourth ray foot with adduction deformity of the hindfoot, cutane …
An unusual form of familial acrocephalosyndactyly.
Young ID, Harper PS. Young ID, et al. J Med Genet. 1982 Aug;19(4):286-8. doi: 10.1136/jmg.19.4.286. J Med Genet. 1982. PMID: 7120317 Free PMC article.
The most characteristic feature in the more severely affected individuals is duplication of the distal phalanx of the hallux. Review of family photographs suggests that the cosmetic outcome in apparently affected infants may be much better than anticipated....
The most characteristic feature in the more severely affected individuals is duplication of the distal phalanx of the hallux. Review …