Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/98257
Type: Artigo de periódico
Title: Unknown Syndrome: Abnormal Fades, Hypothyroidism, Postaxial Polydactyly, And Severe Retardation: A Third Patient
Author: Cavalcanti D.P.
Abstract: Young and Simpson1 in 1987 and Fryns and Moerman2 in 1988 each reported a case of a new unknown syndrome with hypothyroidism, severe global retardation, and abnormal facies, including microcephaly, blepharo-phimosis, bulbous nose, thin upper lip, low set ears, and micrognathia. A male infant with a similar pattern of malformations and postaxial Polydactyly is reported here.
Editor: BMJ Publishing Group
Rights: fechado
Identifier DOI: 10.1136/jmg.26.12.785
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0024331451&partnerID=40&md5=b586ecc0273fa036e4054a6462d84595
Date Issue: 1989
Appears in Collections:Unicamp - Artigos e Outros Documentos

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