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Dergiler / Acta Orthopaedica et Traumatologica Turcica / 2018 / Cilt: 52 - Sayı: 4

A rare case of tibial hemimelia, surgical technique and clinical results

Marco BASSO
Valentina CAMURRİ
Piero FREDİANİ
Silvio BOERO
Sayfa
315–319
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We report a nine-year-old boy with a type IIIa tibial hemimelia, according to the new Paley classification.We describe the x-ray findings, the surgical treatment technique, and the prognostic course of the patient.Descriptions of such cases are very infrequent in the literature and type of treatment is still objectof debate

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Amaç & Hipotez:We report a nine-year-old boy with a type IIIa tibial hemimelia, according to the new Paley classification.We describe the x-ray findings, the surgical treatment technique, and the prognostic course of the patient.Descriptions of such cases are very infrequent in the literature and type of treatment is still objectof debate
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Temel Bulgular & Veri:We report a nine-year-old boy with a type IIIa tibial hemimelia, according to the new Paley classification.We describe the x-ray findings, the surgical treatment technique, and the prognostic course of the patient.Descriptions of such cases are very infrequent in the literature and type of treatment is still objectof debate
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Sonuç & Katkı:We report a nine-year-old boy with a type IIIa tibial hemimelia, according to the new Paley classification.We describe the x-ray findings, the surgical treatment technique, and the prognostic course of the patient.Descriptions of such cases are very infrequent in the literature and type of treatment is still objectof debate
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

We report a nine-year-old boy with a type IIIa tibial hemimelia, according to the new Paley classification.We describe the x-ray findings, the surgical treatment technique, and the prognostic course of the patient.Descriptions of such cases are very infrequent in the literature and type of treatment is still objectof debate

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Bu Makaleye Atıf Yap

BASSO, M., CAMURRİ, V., FREDİANİ, P., BOERO, S. (2018). A rare case of tibial hemimelia, surgical technique and clinical results. Acta Orthopaedica et Traumatologica Turcica, Cilt: 52 - Sayı: 4, 315–319. https://ajindex.com/articles/353515

Kaynakça (3)

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  2. Schoenecker PL, Capelli AM, Millar EA, et al. Congenital longitudinal deficiency of the tibia. J Bone Jt Surg Am. 1989 Feb;71(2):278e287. PMID: 2918013. Clark MW. Autosomal dominant inheritance of tibial meromelia. Report of a kindred. J Bone Jt Surg Am. 1975 Mar;57(2):262e264. PMID: 1112852. Werner P. Ueber einen seltenen Fall von Zwergwuchs. Arch Gynaekol. 1915;104:278e300. https://doi.org/10.1007/BF01705987.
  3. Stevens CA, Moore CA. Tibial hemimelia in Langer- Giedion syndrome-possible gene location for tibial hemimelia at 8q. Am J Med Genet. 1999 Aug 6;85(4): 409e412. https://doi.org/10.1002/(SICI)1096-8628(19990806)85:4 3.0.CO;2-6. PMID: 10398269. Prasad C, Quackenbush EJ, Whiteman D, Korf B. Limb anomalies in DiGeorge and CHARGE syndromes. Am J Med Genet. 1997 Jan 20;68(2):179e181. https:// doi.org/10.1002/(SICI)1096-8628(19970120)68:2 3.0.CO;2-R. PMID: 9028454. Laurin CA, Favreau JC, Labelle P. Bilateral absence of the radius and tibia with bilateral redu-plication of the ulna and fibula: a case report. J Bone Jt Surg Am. 1964 Jan;46:137e142. https://doi.org/10.2106/00004623-196446010-00014. PMID: 14104303. Majewski F, Küster W, ter Haar B, Goecke T. Aplasia of tibia with split-hand/ split-foot de-formity. Report of six families with 35 cases and considerations about variability and penetrance. Hum Genet. 1985;70(2):136e147. PMID: 4007857. Wiedemann HR, Opitz JM. Brief clinical report: unilateral partial tibia defect with preaxial polydactyly, general micromelia, and trigonomacrocephaly with a note on “developmental resistance”. Am J Med Genet. 1983 Mar;14(3): 467e471. https://doi.org/10.1002/ajmg.1320140310. PMID: 6859099. Paley D. Tibial hemimelia: new classification and reconstructive options. J Child Orthop. D