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pubmed-article:21227rdf:typepubmed:Citationlld:pubmed
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pubmed-article:21227pubmed:dateCreated1977-12-29lld:pubmed
pubmed-article:21227pubmed:abstractTextThe authors discuss the nosological position and the aetiology of a complex of malformations affecting a boy, born at the end of a 40-week pregnancy with a weight of 1420 g and height of 42.5 cm, who died at the age of 3 1/2 months. The case presented an association of an acrocephalosyndactyly, phalangeal hypoplasias with anonychia, aplasia of the abdominal muscles, a genital hypoplasia with cryptorchidism and hypospadias, patches of lipodystrophy localised on the outside of the arms, at the folds of the elbow and the popliteal fossae. The autopsy revealed a large interventricular communication, absence of common mesentery and especially important cerebral anomalies (smooth brain, absence of interhemispherical suture, disorganization of the basal ganglia). The genetic study suggested a spontaneous abortion 2 1/2 months before the birth of the patient and revealed, in the mother, the presence of bilateral clinodactylies of the fingers and a unilateral syndactyly of the big toes.lld:pubmed
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pubmed-article:21227pubmed:monthJunlld:pubmed
pubmed-article:21227pubmed:issn0021-7743lld:pubmed
pubmed-article:21227pubmed:authorpubmed-author:FarriauxJ PJPlld:pubmed
pubmed-article:21227pubmed:authorpubmed-author:FontaineGGlld:pubmed
pubmed-article:21227pubmed:authorpubmed-author:LefebvreCClld:pubmed
pubmed-article:21227pubmed:authorpubmed-author:BlanckaertDDlld:pubmed
pubmed-article:21227pubmed:issnTypePrintlld:pubmed
pubmed-article:21227pubmed:volume25lld:pubmed
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pubmed-article:21227pubmed:authorsCompleteYlld:pubmed
pubmed-article:21227pubmed:pagination109-19lld:pubmed
pubmed-article:21227pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:21227pubmed:year1977lld:pubmed
pubmed-article:21227pubmed:articleTitle[A new complex polymalformative syndrome (author's transl)].lld:pubmed
pubmed-article:21227pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21227pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:21227pubmed:publicationTypeCase Reportslld:pubmed