Ring 9 Chromosome Syndrome in Black African Infant

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AuteurALAO, MODJERE OLA MAROUFOU JULES
Date d'ajout2026-06-02T16:06:57Z
Date de disponibilite2026-06-02T16:06:57Z
Date de publication2015
ResumeRing chromosomes are rare entities, usually associated with phenotypic abnormalities in correlation with the loss of genetic material. Ring 9 chromosome syndrome is very rare. The majority of reported cases revealed a less distinct clinical picture of shortness of stature, microcephaly and mental retardation. A minority had the clinical pattern of patients with the deletion of the short arm of chromosome 9 syndrome. We reported here a black female African with malformation and a mixture of major features in ring 9 and deletion of the short arm of chromosome 9 syndrome characteristics upon ring shape by one of chromosome 9 at cytogenetic evaluation.
Autre identifiantBECDB-5513
URIhttps://dspace.uac.bj/handle/123456789/5099
Languefr
Fait partie deJournal of Genetic Disorders & Genetic Reports
Sujetmalformation
SujetGrowth delay
SujetMental retardation
SujetRing 9 chromosome
TitreRing 9 Chromosome Syndrome in Black African Infant
TypeArticle

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