Онтологія вроджених вад скелету кисті

Автор(и)

  • T. V. Khmara
  • Ya. M. Vasylchyshyn
  • A. S. Hresko
  • I. H. Biriuk

DOI:

https://doi.org/10.24061/1727-0847.13.4.2014.21

Ключові слова:

кисть, вада розвитку, анатомія, людина

Анотація

На підставі проведеного аналізу джерел літератури зроблена спроба узагальнити існуючі відомості про вроджені вади скелету кисті та запропоновано їх класифікацію і тлумачення згідно абетки.

Посилання

Dy C.J., Swarup I., Daluiski A. Embryology, diagnosis, and evaluation of congenital hand anomalies. Curr. Rev. Musculoskelet. Med. 2014; 7 (1): 60-67.

Bermejo-Sanchez E., Cuevas L., Amar E. Amelia: a multi-center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. Am. J. Med. Genet. C. Semin. Med. Genet. 2011; 157C (4): 288-304.

Senes F.M., Catena N. Correction of forearm deformities in congenital ulnar club hand: one-bone forearm. J. Hand. Surg. Am. 2012; 37 (1): 159-164.

Puvabanditsin S., Savla J., Garrow E. Symmetrical upper limb peromelia and lower limb amelia associated with persistent omphalomesenteric duct: a case report. Clin. Dysmorphol. 2011; 20 (2): 102-106.

Girsch W., Grill F. Peromelia. Handchir. Mikrochir. Plast. Chir. 2008; 40 (1): 8-12.

Bermejo-Sanchez E., Cuevas L., Amar E. Phocomelia: a worldwide descriptiveepidemiologic study in a large series of cases from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. Am. J. Med. Genet. C. Semin. Med. Genet. 2011; 157C (4): 305-320.

Shetty P., Menezes L.T., Tauro L.F. Amniotic band syndrome. Indian J. Surg. 2013; 75 (5): 401-402.

Suresh S. Robinow syndrome. Indian. J. Orthop. 2008; 42 (4): 474-476.

Patton M., Afzal A. Robinow syndrome. J. Med. Genet. 2002; 39 (5): 305-310.

Pavlova M.N., Belyaeva A.A., Gusev B.V. Vrozhdennyy chastichnyy gigantizm verkhnikh konechnostey u detey [Congenital partial gigantism of the upper limbs of children]. Arkhivy patologii. 1986; 48 (8): 63-68 (in Russian).

Rudenko I.A., Krasnoporov M.M., Shmatko V.Ya. Podovzhennia kistok pry vrodzhenykh ta nabutykh kalitstvakh kysti [Extension of bones in congenital and acquired deformities hand]. Visnyk ortopedii, travmatolohii ta protezuvannia. 2004; 1: 64-67 (in Ukrainian).

Lomachenko I.N., Kozyreva S.P., Pasynkov A.N. Poroki razvitiya paltsev i kisti u detey [Malformations of finger and hand development of children]. Surgery. 1995; 4: 36-37 (in Russian).

Hayes I.M., Varigos G., Upjohn E.J. Unilateral acheiria and fatal primary pulmonary hypertension in a girl with incontinentia pigmenti. Am. J. Med. Genet. A. 2005; 135 (3): 302-303.

Makrythanasis P.,Temtamy S., Aglan M.S. A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly. Hum. Mutat. 2014; 35 (8): 959-963.

Seven M., Yosunkaya E., Guven G. The very rare aglossia adactylia syndrome with a novel finding of mental retardation. Genet Couns. 2012; 23 (1): 81-85.

Chirkova G.N., Sorokina T.V., Novikov N.V. Dva sluchaya sindroma akrotsefalosindaktilii [Two cases of acrocephalosyndactyly syndrome]. Pediatrics. 2003; 3: 100-103 (in Russian).

Inbar-Feigenberg M., Meirowitz N., Nanda D. Beals syndrome (congenital contractural arachnodactyly): prenatal ultrasound findings and molecular analysis. Ultrasound Obstet. Gynecol. 2014; 44 (4): 486-490.

Blauth W., Falliner A. Probleme der operativen Behandlung angeborener Unterschenkel pseudarthrosen. Z. Orthop. Ihre Grenzgeb. 1989; 127 (5): 531-548.

Agranovich O.Ye. Zerkalnaya kist [Mirror hand]. Russian family doctor. 2006; 10: 13-16 (in Russian).

Al-Qattan М., Al-Thunayan A., De Cordier M. Classification of the mirror hand – multiple hand spectrum. J. Hand Surg. 1998; 23B (4): 534-536.

Al-Qattan М., Hashem F.K., Al Malaq A. An unusual case of preaxial polydactyly of the hands and feet: a case report. J. Hand Surg. 2002; 27A (3): 498-502.

Chinegwundon J.O.M., Gupta M., Scott A. Ulnar dimelia. Is it a true duplication of the ulna? J. Hand Surg. 1997; 22B (1): 77-79.

Sandrow R.E., Sullivan P.D., Steel H.H. Hereditary ulnar and fibular dimelia with peculiar facies. A case report. J. Bone Jt. Surg. 1970; 52A (2): 367-370.

Martin R.A., Jones M.C., Jones K.L. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition. Am. J. Med. Genet. 1993; 46 (2): 129-131.

Shvedovchenko I.V., Bergaliev A.N., Sosnenko O.N. Kliniko-radiologicheskie paralleli pri vrozhdennom gigantizme kisti u detey [Clinical and radiological parallels with congenital gigantism of the hand of children]. Vestnik travmatologii i ortopedii im. N.N. Priorova. 2002; 1: 20-25 (in Russian).

Dhar R.S., Bora A. Ectrodactyly-ectodermal dysplasia-cleft lip and palate syndrome. J. Indian. Soc. Pedod. Prev. Dent. 2014; 32 (4): 346-349.

Mitul B. K., Avani A.S. A Case of Ectrodactyly in a Neonate. J. Clin. Neonatol. 2013: 2 (3): 151-152.

Shivaprakash P.K., Hrishikesh Joshi V., Noorani H. Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome: A case report of “Incomplete syndrome”. Contemp. Clin. Dent. 2012; 3 (1): 115-117.

Kenkare S., Ainapurapu B. Macrodactylia fibrolipomatosis presenting as a small bowel obstruction. South Med. J. 2010; 103 (7): 721.

Nguyen M.P., Lawler E.A., Morcuende J.A. A case report of bilateral mirror clubfeet and bilateral hand polydactyly. Iowa Orthop. J. 2014; 34: 171-174.

Wang C., Huang X., Tan W. A new skill for treating unclassified thumb polydactyly: ablation via a periosteal incision. Aesthetic Plast. Surg. 2012; 36 (4): 928-933.

Khode S.R., Gosrani N., Golhar S. Congenital vallecular cyst with polydactyly – A rare cause of stridor and failure to thrive. Med. J. Malaysia. 2014; 69 (2): 101-102.

Wood V.E. Treatment of the triphalangeal thumb. Clin. Orthop. 1976; 120: 188-200.

Wood V.E. Polydactyly and the triphalangeal thumb. J. Hand. Surg. Am. 1978; 3 (5): 436-444.

Wood V.E., Flatt A.E. Congenital triangular bones in the hand. J. Hand. Surg. Am. 1977; 2 (3): 179-193.

Agranovich O.Ye., Shvedovchenko I.V., Golyana S.I. Teratologicheskie varianty vrozhdennogo trekhfalangizma I paltsa kisti u detey [Terato logical variants of congenital trifalangism of the first finger of the hand in children]. Vestnik travmatologii i ortopedii im. N.N. Priorova. 2003; 4: 80-83 (in Russian).

Agranovich O.Ye. Vrozhdennaya gipoplaziya І lucha kisti [Congenital hypoplasia of the first ray of the hand]. Russian Journal of Pediatric Surgery. 2009; 3: 42-46 (in Russian).

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2014-12-24

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