Aplasia Fibular
Mostrando 1-3 de 3 artigos, teses e dissertações.
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1. Estudos moleculares em famílias com defeitos de membros / Molecular studies in families with limb defects
No presente trabalho foram desenvolvidos estudos genético-moleculares em três famílias com três síndromes distintas de defeitos dos membros. A ectrodactilia ou SHFM (split-hand/split-foot malformation) é uma malformação congênita da extremidade dos membros caracterizada por fenda mediana profunda das mãos e/ou pés devido à ausência dos raios cen
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 25/04/2011
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2. Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects.
Multiple vertebral segmentation defects occur in a group of conditions variably associated with anomalies of other organ systems. This report describes a female child in whom a deletion of chromosome 18 (18q22.2-->qter) is associated with congenital anomalies including multiple vertebral segmentation defects resembling sporadic spondylocostal dysplasia. The
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3. The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.
A case is reported where the major clinical features of craniostenosis and radial aplasia led to an initial diagnosis of Baller-Gerold syndrome. Mild fibular hypoplasia on skeletal survey led to review of the diagnosis and the similarity of the facial phenotype to that of Roberts syndrome was noted. Chromosome analysis showed the premature centromere separat