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Biomedical subjects

S Elias

Publications and source records attributed to S Elias.

225 records · Page 13Linked to original sources
PubMedDate not supplied

Molecular analysis to assign parental origin and distinguish de novo i(21q) from t(21q21q) in two Down syndrome fetuses.

OBJECTIVE: We sought to determine the origin of two prenatal cases of chromosome 21 rearrangements not amenable to clarification by conventional cytogenetic methodology. METHODS: Hypervariable repeat polymorphisms (chromosome 21) were used to determine the type of structural rearrangement and the parental origin of the rearranged chromosome. The repeats used were highly polymorphic and located very close to the centromere; thus, the likelihood of differences among the parental alleles and overall informativeness were increased. RESULTS: The rea(21q21q) chromosomes were identified as a Robertsonian translocation in one fetus and an isochromosome in the other. The extra chromosome material was found to be maternal in origin in both cases. CONCLUSION: The ability to clarify the origin of abnormal chromosomal rearrangements provides valuable information concerning possible mechanisms of aneuploidy, as well as clinical data that may have an impact in assessing a patient's risk for abnormal offspring.

Chromosomes, Human, Pair 21↗
PubMedDate not supplied

Cytogenetic analysis of a case of "13q- syndrome" (46,XX,del 13) using banding techniques.

Many chromosomal syndromes include ocular anomalies. In the del(13q) syndrome retinoblastoma, coloboma, and microphthalmia may be present. In the del(13q) case we report, the findings include colobomas and apparent microphthalmia, although the retinoblastoma sometimes associated with this condition was not observed. More precise descriptions of the del(13q) syndrome relative to the region deleted using improved banding techniques may: (1) increase the likelihood of accurate diagnosis, (2) enhance clinical predictions, and (3) possibly further clarify the genetic control over the development of the ocular system.

Abnormalities, Multiple↗
PubMedDate not supplied

Adventitial cystic disease.

Adventitial cystic disease is a rare syndrome predominantly seen in young males with the acute onset of claudication. Early diagnosis and confirmation with arteriography is of utmost importance to the success of treatment. The authors present a rare case report and treatment of adventitial cystic disease.

Adult↗
PubMedDate not supplied

[Detection of fetal cells in maternal blood: towards a noninvasive prenatal diagnosis].

Fetal cells exist in maternal blood and can be utilized for prenatal genetic diagnosis. These cells are present during the first and second trimesters, with frequency increasing as gestation advances. Enrichment of erythroblasts by various density gradient techniques and either magnetic activated or flow sorting techniques can be followed by FISH with chromosome-specific DNA probes. This approach has allowed detection of trisomy 21, trisomy 18, Klinefelter syndrome 47,XXY and 47,XYY. Polymerase chain reaction (PCR) analysis of maternal blood has enabled the detection of fetal sex, certain Mendelian disorders (e.g. beta-globin mutations), HLA polymorphisms, and fetal Rhesus (D) blood type. The fetal cell types receiving the most attention has been nucleated erythrocyte (erythroblast) and the trophoblast. Lymphocytes and granulocytes are also present in maternal blood; however, lymphocytes are considered the cell type most likely to persist after pregnancy. A large scale collaborative is now underway in the U.S. that will allow determine whether sensitivity and specificity of this technique provide a noninvasive alternative to conventional methods of prenatal cytogenetic diagnosis.

Cell Separation↗