Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/193620
Type: Artigo de periódico
Title: Unknown Syndrome: Abnormal Facies, Hypothyroidism, Postaxial Polydactyly, And Severe Retardation: A Third Patient.
Author: Cavalcanti, D P
Abstract: Young and Simpson in 1987 and Fryns and Moerman in 1988 each reported a case of a new unknown syndrome with hypothyroidism, severe global retardation, and abnormal facies, including microcephaly, blepharophimosis, 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.
Subject: Abnormalities, Multiple
Congenital Hypothyroidism
Facial Bones
Fingers
Humans
Infant
Infant, Newborn
Intellectual Disability
Male
Skull
Syndrome
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/2614801
Date Issue: 1989
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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