GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA

Detalhes bibliográficos
Autor(a) principal: Freiere Maia, A.
Data de Publicação: 1974
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/230757
Resumo: Acheiropodia is a congenital malformation with well defined characteristics and well established genetic etiology. It is proposed that the expression 'acheiropodia' be restricted exclusively to such cases and others that follow the definition. Several examples are given which do not agree with the concept; therefore, they should not be confounded with cases of acheiropodia. By analogy with what happens in acheiropodia, it is proposed that the expression 'acheiria' be restricted to those cases where the anomaly affects only the upper limbs and follows the same typical pattern of acheiropodia. A family analysis of one such case is mentioned, but there is not sufficient information to test the hypothesis of a simple genetic mechanism.
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spelling GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIAGenetics of acheiropodia (the handless and footless families of Brazil). II: Acheiria and cases 'similar' to acheiropodiaAcheiropodia is a congenital malformation with well defined characteristics and well established genetic etiology. It is proposed that the expression 'acheiropodia' be restricted exclusively to such cases and others that follow the definition. Several examples are given which do not agree with the concept; therefore, they should not be confounded with cases of acheiropodia. By analogy with what happens in acheiropodia, it is proposed that the expression 'acheiria' be restricted to those cases where the anomaly affects only the upper limbs and follows the same typical pattern of acheiropodia. A family analysis of one such case is mentioned, but there is not sufficient information to test the hypothesis of a simple genetic mechanism.Dept. Genet., Fac. Ci. Med. Biol., Botucatu2022-04-29T08:41:55Z2022-04-29T08:41:55Z1974-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article107-110Revista Paulista de Medicina, v. 84, n. 3-4, p. 107-110, 1974.0035-0362http://hdl.handle.net/11449/2307572-s2.0-0016231741Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporRevista Paulista de MedicinaFreiere Maia, A.info:eu-repo/semantics/openAccess2022-04-29T08:41:55Zoai:repositorio.unesp.br:11449/230757Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T08:41:55Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
Genetics of acheiropodia (the handless and footless families of Brazil). II: Acheiria and cases 'similar' to acheiropodia
title GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
spellingShingle GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
Freiere Maia, A.
title_short GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
title_full GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
title_fullStr GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
title_full_unstemmed GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
title_sort GENETICA DA AQUIROPODIA ('THE HANDLESS AND FOOTLESS FAMILIES OF BRAZIL') II: AQUIRIA E CASOS 'SIMILARES' A AQUIROPODIA
author Freiere Maia, A.
author_facet Freiere Maia, A.
author_role author
dc.contributor.author.fl_str_mv Freiere Maia, A.
description Acheiropodia is a congenital malformation with well defined characteristics and well established genetic etiology. It is proposed that the expression 'acheiropodia' be restricted exclusively to such cases and others that follow the definition. Several examples are given which do not agree with the concept; therefore, they should not be confounded with cases of acheiropodia. By analogy with what happens in acheiropodia, it is proposed that the expression 'acheiria' be restricted to those cases where the anomaly affects only the upper limbs and follows the same typical pattern of acheiropodia. A family analysis of one such case is mentioned, but there is not sufficient information to test the hypothesis of a simple genetic mechanism.
publishDate 1974
dc.date.none.fl_str_mv 1974-01-01
2022-04-29T08:41:55Z
2022-04-29T08:41:55Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Revista Paulista de Medicina, v. 84, n. 3-4, p. 107-110, 1974.
0035-0362
http://hdl.handle.net/11449/230757
2-s2.0-0016231741
identifier_str_mv Revista Paulista de Medicina, v. 84, n. 3-4, p. 107-110, 1974.
0035-0362
2-s2.0-0016231741
url http://hdl.handle.net/11449/230757
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista Paulista de Medicina
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 107-110
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1799965197523222528

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