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1.
Rev. bras. ortop ; 47(5): 545-552, set.-out. 2012. ilus, tab
Article in Portuguese | LILACS | ID: lil-660902

ABSTRACT

Este artigo, dividido em três partes, tem por objetivo rever as deformidades congênitas mais comuns que afetam os membros superiores e descrever seus tratamentos. Nesta primeira parte, discute-se as falhas de formação. A bibliografia segue contínua a partir da primeira parte.


This article, divided into three parts, had the aims of reviewing the most common upper-limb malformations and describing their treatments. In this first part, failure of formation is discussed. The bibliography follows after the first part.


Subject(s)
Humans , Congenital Abnormalities , Upper Extremity Deformities, Congenital/history , Upper Extremity
2.
Surg Radiol Anat ; 34(2): 101-6, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22068244

ABSTRACT

For years people have been enamored by anomalies of the human limbs, particularly supernumerary and absent limbs and digits. Historically, there are a number of examples of such anomalies, including royal families of ancient Chaldea, tribes from Arabia, and examples from across nineteenth century Europe. The development of the upper limbs in a growing embryo is still being elucidated with the recent advent of homeobox genes, but researchers agree that upper limbs develop between stages 12-23 through a complex embryological process. Maternal thalidomide intake during limb development is known to cause limb reduction and subsequent amelia or phocomelia. Additionally, a number of clinical reports have illustrated different limb anomaly cases, with each situation unique in phenotype and developmental abnormality. Supernumerary and absent limbs and digits are not unique to humans, and a number of animal cases have also been reported. This review of the literature illustrates the historical, anatomical, and clinical aspects of supernumerary and absent limbs and digits for the upper limb.


Subject(s)
Ectromelia/diagnosis , Upper Extremity Deformities, Congenital/diagnosis , Upper Extremity/anatomy & histology , Upper Extremity/embryology , Ectromelia/epidemiology , Ectromelia/history , Female , History, 18th Century , History, 19th Century , History, Ancient , Humans , Incidence , Male , Polydactyly/diagnosis , Polydactyly/epidemiology , Polydactyly/history , Upper Extremity Deformities, Congenital/epidemiology , Upper Extremity Deformities, Congenital/history , West Indies/epidemiology
3.
ANZ J Surg ; 81(12): 900-4, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22507417

ABSTRACT

Born in Edinburgh in 1774 Sir Charles Bell, as a young man, studied anatomy and surgery in his hometown. There followed a distinguished career that culminated in his becoming the first professor of Anatomy and Surgery at the College of Surgeons in London. Renowned as a brilliant neuroanatomist he was invited, on the advice of His Grace the Archbishop of Canterbury and the Bishop of London, to contribute one of eight volumes of a work on the Power Wisdom and Goodness of God as manifested in the Creation - known as the Bridgewater Treatises. 'The Hand its Mechanism and Vital Endowments as Evincing Design' was published in 1833 and it is an account of his considering the hand as a machine that has been engineered to exacting standards to interact with the environment in which we live. In it he expressed a deep understanding of the similarity of the structure of the upper limbs of the higher orders of animals. The similarity of the paddle of a turtle and a human hand with acrosymbrachydactyly is unmistakable. This congenital abnormality, given the eponymous title of Apert's syndrome, is one of a number of congenital abnormalities that have parallels in the animal kingdom. Others who have had similar syndromes named after them include Poland, Marfan, Streeter and a number of others. The life and times of these men and their contributions to medicine will be presented in this paper.


Subject(s)
Anatomy/history , General Surgery/history , Upper Extremity Deformities, Congenital/history , Ehlers-Danlos Syndrome/history , History, 18th Century , History, 19th Century , History, 20th Century , Humans , Marfan Syndrome/history , Syndactyly/history , United Kingdom
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