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Classification and surgical treatment of symphalangism in interphalangeal joints of the hand.
Baek GH, Lee HJ. Baek GH, et al. Clin Orthop Surg. 2012 Mar;4(1):58-65. doi: 10.4055/cios.2012.4.1.58. Epub 2012 Feb 20. Clin Orthop Surg. 2012. PMID: 22379556 Free PMC article.
Here, we report our experiences on surgical treatment for children who had symphalangism of the hand. METHODS: We treated 36 joints in 17 children with symphalangism of the hand using dorsal capsulotomy and collateral ligament release. ...The final ROM was significa …
Here, we report our experiences on surgical treatment for children who had symphalangism of the hand. METHODS: We treated 36 joints i …
Prolonged Union in Conservative Treatment of Symphalangeal Toe Fractures: Case Series.
Kyung MG, Yoon YS, Kim Y, Lee KM, Lee DY, Hwang IU. Kyung MG, et al. Clin Orthop Surg. 2024 Apr;16(2):322-325. doi: 10.4055/cios23174. Epub 2024 Feb 16. Clin Orthop Surg. 2024. PMID: 38562628 Free PMC article.
BACKGROUND: Toe symphalangism is characterized by a fusion of the interphalangeal joint between the middle and distal phalanges. ...
BACKGROUND: Toe symphalangism is characterized by a fusion of the interphalangeal joint between the middle and distal phalange …
Twenty-four cases of the EEC syndrome: clinical presentation and management.
Buss PW, Hughes HE, Clarke A. Buss PW, et al. J Med Genet. 1995 Sep;32(9):716-23. doi: 10.1136/jmg.32.9.716. J Med Genet. 1995. PMID: 8544192 Free PMC article.
The presence of hypohidrosis was not noted as a predominant feature in the syndrome and its occurrence appeared to depend on the presence of all other features. Distal limb defects from simple syndactyly to tetramelic cleft hand and foot were identified, including p …
The presence of hypohidrosis was not noted as a predominant feature in the syndrome and its occurrence appeared to depend on the presence of …
Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.
Elliott AM, Evans JA. Elliott AM, et al. Am J Med Genet A. 2006 Jul 1;140(13):1419-27. doi: 10.1002/ajmg.a.31244. Am J Med Genet A. 2006. PMID: 16688749
The deficiency in SHFM patients can also be accompanied by other distal limb anomalies including polydactyly and/or syndactyly. This variability causes the phenotypic classification of SHFM to be far from straightforward and genetic heterogeneity, with at least five …
The deficiency in SHFM patients can also be accompanied by other distal limb anomalies including polydactyly and/or syndactyly …