Experience in Treatment of Total Hand Syndactyly in a Child with Apert Syndrome

O. V Kozhevnikov , A. V Ivanov , Yu. V Gavrilova

N.N. Priorov Journal of Traumatology and Orthopedics ›› 2014, Vol. 21 ›› Issue (4) : 70 -73.

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N.N. Priorov Journal of Traumatology and Orthopedics ›› 2014, Vol. 21 ›› Issue (4) : 70 -73. DOI: 10.17816/vto20140470-73
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Experience in Treatment of Total Hand Syndactyly in a Child with Apert Syndrome

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Abstract

Experience in surgical treatment of total hand syndactyly in a child with Apert syndrome is presented. Surgical technique that includes the application of МЦТ-01 apparatus, distraction period and interdigital space formation with local tissues, i.e. interchanging triangular or oblique-trapeziform flaps is described. Within 18 months interdigital spaces between II and III, III and IV, IV and V fingers were formed in turn. Besides marked cosmetic effect comparatively good functional result was achieved.

Keywords

Apert syndrome / acrocephalosyndactyly / syndactyly / skin plasty / distraction apparatus / distraction

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O. V Kozhevnikov, A. V Ivanov, Yu. V Gavrilova. Experience in Treatment of Total Hand Syndactyly in a Child with Apert Syndrome. N.N. Priorov Journal of Traumatology and Orthopedics, 2014, 21(4): 70-73 DOI:10.17816/vto20140470-73

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References

[1]

Козлова С.И., Демикова Н.С. Наследственные синдромы и медико-генетическое консультирование. М.: Медицина; 2007: 20-2.

[2]

Apert E. De l’acrocéphalosyndactylie. Bulletins et mémoires de la Société medicale des hôpitaux de Paris, 1906; 23: 1310-30.

[3]

Tolarova M.M., Harris J.A., Ordway D.E., Vargervik K. Birth prevalence, mutation rate, sex ratio, parents’age, and ethnicity in Apert syndrome. Am. J. Med. Genet. 1997; 72 (4): 394-8;

[4]

Tanimoto Y1., Yokozeki M., Hiura K, Matsumoto K., Nakanishi H., Matsumoto T., Marie P.J., Moriyama K. A soluble form of fibroblast growth factor receptor 2 (FGFR2) with S252W mutation acts as an efficient inhibitor for the enhanced osteoblastic differentiation caused by FGFR2 activation in Apert syndrome. J. Biol. Chem. 2004; 279 (44): 45926-34.

[5]

Ясонов С.А., Лопатин А.В., Маслов В.В., Васильев И.Г., Быстров А.В. Cиндром Апера (Аpert): современные возможности комплексного реконструктивного лечения. Детская больница. 2011; 2: 51-4.

[6]

Чиркова Г.Н., Сорокина Т.В., Новиков Н.В. Два случая синдрома акроцефалосиндактилии. Педиатрия. 2003; 5: 100-3.

[7]

Upton J. Apert Syndrome. Classification and pathologic anatomy of limb anomalies. Clinics in plastic surgery. 1991; 18 (2): 321-55.

[8]

Кожевников О.В., Иванов А.В., Гаврилова Ю.В. Наш опыт лечения синдактилий пальцев кисти у детей с использованием компрессионно-дистракционного метода. В кн.: Сборник тезисов II конгресса травматологов и ортопедов «Травматология и ортопедия столицы: настоящее и будущее». М.; 2014: 130-1.

[9]

Кожевников О.В., Иванов А.В., Гаврилова Ю.В. Возможности компрессионно-дистракционного метода в лечении тяжелых форм врожденных синдактилий кисти. В кн.: Материалы III научно-практической конференции хирургов кисти Уральского региона. Курган; 2014: 24-5.

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