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Cytogenetic diagnosis of Roberts SC phocomelia syndrome: first report from Kashmir
Egyptian Journal of Medical Human Genetics [The]. 2016; 17 (1): 137-140
em Inglês | IMEMR | ID: emr-176226
ABSTRACT
There are several syndromes in which specific mitotic chromosomal abnormalities can be seen, like premature centromere separation, premature [sister] chromatid separation, and somatic aneuploidies. Identifications of such specific cytogenetic findings can be the key factor that leads towards the diagnosis of syndromes like Roberts SC phocomelia. The case presented here as Roberts SC phocomelia syndrome was identified as a child with multiple congenital anomalies and dysmorphic features. Conventional cytogenetic analysis of the case revealed premature sister chromatid separation. The premature centromeric separation was also confirmed by C banding analysis of the child. It is the first and the only case of Roberts SC phocomelia diagnosed from this part of the world. The present case report emphasizes the importance of conventional cytogenetics in the diagnosis of such syndromes
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Centrômero / Cromátides / Anormalidades Craniofaciais / Citogenética / Hipertelorismo / Aneuploidia Tipo de estudo: Relato de Casos Limite: Criança, pré-escolar / Feminino / Humanos Idioma: Inglês Revista: Egypt. J. Med. Hum. Genet. Ano de publicação: 2016

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Centrômero / Cromátides / Anormalidades Craniofaciais / Citogenética / Hipertelorismo / Aneuploidia Tipo de estudo: Relato de Casos Limite: Criança, pré-escolar / Feminino / Humanos Idioma: Inglês Revista: Egypt. J. Med. Hum. Genet. Ano de publicação: 2016