RESUMO
Karyotyping couples that have had recurrent miscarriages detects balanced rearrangements in carrier parents who can be offered prenatal cytogenetic analysis to prevent the birth of a subsequent child with an unbalanced rearrangement. In four UK centres, over periods of 5-30 years, balanced rearrangements were found in 406 out of 20,432 parents that had experienced miscarriage (1.9%), but only four unbalanced rearrangements were found after referral for prenatal diagnosis because of a balanced parental translocation ascertained for recurrent miscarriages. At an estimated cost of 3-4 million pounds, these data raise doubts about the cost effectiveness of current policies on the routine karyotyping of couples experiencing repeated miscarriages.
Assuntos
Aborto Habitual/genética , Transtornos Cromossômicos/diagnóstico , Cariotipagem , Diagnóstico Pré-Natal/economia , Aborto Habitual/prevenção & controle , Transtornos Cromossômicos/genética , Análise Custo-Benefício , Feminino , Humanos , Gravidez , Estudos RetrospectivosRESUMO
We report a 21-week gestation fetus terminated because of multiple congenital abnormalities seen on ultrasound scan, including ventriculomegaly, possible clefting of the hard palate, cervical hemivertebrae, micrognathia, abnormal heart, horseshoe kidney and a 2-vessel umbilical cord. On cytogenetic examination, the fetus was found to have a male karyotype with 45 chromosomes with a dicentric chromosome, which appeared to consist of the long arms of chromosomes 13 and 17. Molecular genetic investigations and fluorescence in situ hybridization (FISH) unexpectedly showed that the derivative chromosome contained two interstitial blocks of chromosome 17 short arm sequences, totalling approximately 7 Mb, between the two centromeres. This effectively made the fetus monosomic for approximately 15 Mb of 17p without the concurrent trisomy for another chromosome normally seen following malsegregation of reciprocal translocations. It also illustrates the complexity involved in the formation of some structurally abnormal chromosomes, which can only be resolved by detailed molecular investigations.
Assuntos
Anormalidades Múltiplas/embriologia , Anormalidades Múltiplas/genética , Aberrações Cromossômicas , Cromossomos Humanos Par 13 , Cromossomos Humanos Par 17 , Anormalidades Múltiplas/diagnóstico por imagem , Aborto Induzido , Adulto , Mapeamento Cromossômico , Feminino , Idade Gestacional , Humanos , Hibridização in Situ Fluorescente , Cariotipagem , Masculino , Gravidez , Deleção de Sequência , Pele/embriologia , UltrassonografiaRESUMO
We report on a man with mental retardation and a complex karyotype with cells containing up to three morphologically distinct supernumerary marker chromosomes (SMCs) in most metaphases. Fluorescence in situ hybridisation studies using chromosome 15-specific probes characterised the presence of seven SMCs all derived from chromosome 15. The results suggest that the patient originally had a large inv dup(15) containing two copies of the Prader-Willi/Angelman critical region which became mitotically unstable, and by a process of dynamic mosaicism various morphologically distinct SMCs arose.
Assuntos
Síndrome de Angelman/genética , Cromossomos Humanos Par 15/genética , Mosaicismo/genética , Síndrome de Prader-Willi/genética , Adulto , Síndrome de Angelman/diagnóstico , Aberrações Cromossômicas , Inversão Cromossômica , Sondas de DNA/genética , Feminino , Humanos , Hibridização in Situ Fluorescente , Cariotipagem , Linfócitos , Masculino , Mosaicismo/diagnóstico , Síndrome de Prader-Willi/diagnósticoAssuntos
Anormalidades Múltiplas/genética , Aberrações Cromossômicas/genética , Cromossomos Humanos Par 3/genética , Feto/anormalidades , Duplicação Gênica , Anormalidades Múltiplas/diagnóstico por imagem , Aborto Eugênico , Adulto , Aberrações Cromossômicas/diagnóstico por imagem , Transtornos Cromossômicos , Feminino , Fibroblastos , Dosagem de Genes , Marcadores Genéticos/genética , Humanos , Hibridização in Situ Fluorescente , Cariotipagem , Masculino , Gravidez , Diagnóstico Pré-Natal , UltrassonografiaRESUMO
A de novo dicentric Y;21 (q11.23;p11) translocation chromosome with one of its two centromeres inactive has provided the opportunity to study the relationship between centromeric inactivation, the organization of alphoid satellite DNA and the distribution of CENP-C. The proband, a male with minor features of Down's syndrome, had a major cell line with 45 chromosomes including a single copy of the translocation chromosome, and a minor one with 46 chromosomes including two copies of the translocation chromosome and hence effectively trisomic for the long arm of chromosome 21. Centromeric activity as defined by the primary constriction was variable: in most cells with a single copy of the Y;21 chromosome, the Y centromere was inactive. In the cells with two copies, one copy had an active Y centromere (chromosome 21 centromere inactive) and the other had an inactive Y centromere (chromosome 21 centromere active). Three different partial deletions of the Y alphoid array were found in skin fibroblasts and one of these was also present in blood. Clones of single cell origin from fibroblast cultures were analysed both for their primary constriction and to characterise their alphoid array. The results indicate that (1) each clone showed a fixed pattern of centromeric activity; (2) the alphoid array size was stable within a clone; and (3) inactivation of the Y centromere was associated with both full-sized and deleted alphoid arrays. Selected clones were analysed with antibodies to CENP-C, and staining was undetectable at both intact and deleted arrays of the inactive Y centromeres. Thus centromeric inactivation appears to be largely an epigenetic event.
Assuntos
Cromossomos Humanos Par 21/genética , Translocação Genética , Cromossomo Y/genética , Adolescente , Centrômero/genética , Centrômero/metabolismo , Centrômero/ultraestrutura , Proteínas Cromossômicas não Histona/metabolismo , Cromossomos Humanos Par 21/metabolismo , Cromossomos Humanos Par 21/ultraestrutura , Células Clonais , Citogenética , DNA Satélite/genética , Síndrome de Down/genética , Síndrome de Down/metabolismo , Humanos , Hibridização in Situ Fluorescente , Masculino , Fenótipo , Cromossomo Y/metabolismo , Cromossomo Y/ultraestruturaRESUMO
Gonadal dysgenesis resulting in primary infertility is one of the most common features of Turner syndrome. There have been a number of cases described of pregnancy in 45,X subjects, but whether or not the fertility is associated with a 46,XX cell line in the germ cells is not known. We describe a 45,X/46,X,psu idic(Xq) female with normal fertility, in whom a cryptic 46,XX cell line was found in the germ cells.
Assuntos
Síndrome de Turner , Cromossomo X , Adulto , Linhagem da Célula , Feminino , Fertilidade/genética , Células Germinativas , Humanos , Recém-Nascido , Cariotipagem , Masculino , GravidezRESUMO
Thirty perinatal solid tissue samples were used in a pilot study to test the efficacy of collagenase disaggregation onto coverslips, open system culture under low O2 conditions, pre-harvest incubation in bromodeoxyuridine (BrdU) and colcemid, and in situ automated harvesting. Following the success of the pilot study, the new method was applied to a further 126 consecutive diagnostic samples making a total of 156. The method reduced average tissue culture times from 17 to 8.7 days (range 2-17), improved success rates from 76 to 88 per cent, and simultaneously increased the resolution of cytogenetic analysis.
Assuntos
Bandeamento Cromossômico/métodos , Colagenases/metabolismo , Técnicas de Preparação Histocitológica , Âmnio/patologia , Biópsia , Técnicas de Cultura/métodos , Desenvolvimento Embrionário e Fetal/fisiologia , Feminino , Humanos , Músculos/embriologia , Músculos/patologia , Ovário/embriologia , Ovário/patologia , Projetos Piloto , Placenta/patologia , Gravidez , Pele/embriologia , Pele/patologia , Fatores de Tempo , Cordão Umbilical/patologiaRESUMO
We report a reciprocal translocation t(8;18)(p21.3;p11.23) in which both unbalanced products of adjacent 1 segregation were observed within a family. The proband was originally referred because of short stature and a webbed neck, but further investigations showed that she had mental retardation and a congenital heart defect, and had inherited an unbalanced form of the maternal translocation, 46, XX,der(8)t(8;18)mat. The proband's sister spontaneously aborted an 11 week fetus with multiple major system malformations, which was found to have a 46,XY, der(18)t(8;18)mat karyotype. The phenotypic findings of the affected subjects are discussed.
Assuntos
Cromossomos Humanos Par 18 , Cromossomos Humanos Par 8 , Translocação Genética , Adolescente , Feminino , Humanos , Masculino , LinhagemRESUMO
We describe the first case of maternal uniparental disomy (UPD) of chromosome 9 in a fetus who was shown to have mosaic trisomy 9 in a chorionic villus sample. Karyotyping and molecular studies following termination of the pregnancy confirmed mosaicism in the placenta and maternal UPD(9) in the fetal tissues. This case demonstrates that the mechanism of trisomy correction may result in a fetus with UPD(9).
Assuntos
Amostra da Vilosidade Coriônica , Cromossomos Humanos Par 9/genética , Mosaicismo , Placenta , Trissomia/genética , Aborto Induzido , Adulto , Citogenética , Feminino , Impressão Genômica , Humanos , Hibridização in Situ Fluorescente , Cariotipagem , Biologia Molecular , Reação em Cadeia da Polimerase , GravidezRESUMO
X inactivation analysis was performed on normal and hypopigmented skin samples obtained from a female with hypomelanosis of Ito associated with a balanced whole arm X;17 translocation. Severe skewing of X inactivation resulting in inactivity of the intact X was found in blood and cultures of both types of skin, but analysis of DNA prepared directly from hypopigmented skin showed significant inactivation of the translocated X, inconsistent with the usual mechanism of phenotypic expression in X;autosome translocations. In addition, dual colour FISH analysis using centromere specific probes for chromosomes X and 17 showed that the breakpoints on both chromosomes lie within the alphoid arrays, making interruption of a locus on either chromosome unlikely. While partial variable monosomy of loci on chromosome 17p cannot be excluded as contributing to the phenotype in this patient, it is argued that the major likely factor is partial functional disomy of sequences on Xp in cell lineages that have failed to inactivate the intact X chromosome.
Assuntos
Deleção Cromossômica , Cromossomos Humanos Par 17 , Transtornos da Pigmentação/genética , Receptores Androgênicos/genética , Translocação Genética , Cromossomo X , Adulto , Sequência de Bases , Mapeamento Cromossômico , DNA/sangue , Primers do DNA , Feminino , Humanos , Cariotipagem , Linfócitos , Dados de Sequência Molecular , Transtornos da Pigmentação/sangue , Transtornos da Pigmentação/patologia , Reação em Cadeia da Polimerase , Polimorfismo Genético , Mapeamento por Restrição , Pele/patologiaAssuntos
Cromossomos Humanos Par 18/genética , Mosaicismo , Trissomia , Adulto , DNA/análise , Feminino , Humanos , FenótipoRESUMO
In this study, the clinical, IQ, and cytogenetic findings in nine Turner's syndrome patients with a ring (X) cell line are compared with those in 16 patients in whom only a 45,X cell line could be found. The ring (X) patients lacked many of the "classic" Turner's syndrome features and the majority were not karyotyped until after the age of 11, usually because of pubertal failure. They also showed a reduction in IQ of 11 points compared with the 45,X group. Some ring (X) patients show characteristic facial features including a broad nose with anteverted nostrils, prominent philtrum, long palpebral fissures, and a wide mouth with a thin upper lip. Neither the physical features nor the IQ are related to the parental origin of the chromosome error. In the majority of cases the ring (X) chromosome was late replicating but XIST activity is being studied further.
Assuntos
Cromossomos em Anel , Síndrome de Turner/genética , Cromossomo X/genética , Adolescente , Criança , Pré-Escolar , Citogenética , Feminino , Humanos , Lactente , Fenótipo , Síndrome de Turner/fisiopatologiaRESUMO
Blood samples from 43 infants with Down's syndrome and from 67 with a normal karyotype were screened for the presence of cells positive for platelet glycoproteins GpIb and GpIIIa. There was 1 case of fatal leukaemia and 1 case of transient leukaemia among the Down's syndrome patients, both cases had increased numbers of circulating blood cells positive for platelet glycoprotein markers. These cells were present in small numbers in both the Down's and control groups, especially among stillbirths, and there was no difference in the numbers of such cells found in Down's syndrome patients in comparison with the controls.
Assuntos
Síndrome de Down/sangue , Glicoproteínas da Membrana de Plaquetas/sangue , Medula Óssea/química , Células-Tronco Hematopoéticas/química , Humanos , Lactente , Recém-Nascido , Megacariócitos/químicaRESUMO
The family of a male with Duchenne muscular dystrophy (DMD) and a deletion within the dystrophin gene has been studied. Polymerase chain reaction analysis of ectopic mRNA from peripheral blood T+B lymphocytes and the use of (CA)n repeat polymorphisms in and around the deleted region showed the proband's mother to be both a germline mosaic and a somatic mosaic for the deletion seen in her son. The mutation therefore occurred as a mitotic event early in embryogenesis.
Assuntos
Heterozigoto , Mosaicismo , Distrofias Musculares/genética , Pré-Escolar , Distrofina/genética , Feminino , Deleção de Genes , Mutação em Linhagem Germinativa , Humanos , Células Híbridas , Masculino , Linhagem , Reação em Cadeia da Polimerase , RNA Mensageiro/genéticaRESUMO
Three patients with mosaicism and a cell line containing a small ring (X) chromosome are described. Their phenotype is similar to several previously reported patients with a 45,X/46,X,r(X) karyotype and a phenotype far more severely affected than expected in Turner's syndrome. The clinical picture includes mental retardation, a facial appearance reminiscent of the Kabuki make up syndrome, and limb anomalies. Some of the patients also had streaky hyperpigmentation of the skin in a pattern suggesting dermal mosaicism. It has been hypothesised that the severe phenotype might be the result of the small r(X) chromosome remaining active. However, there is little critical evidence to support this suggestion, while there is considerable evidence against it, including (1) a similar phenotype in 45,X/46,X,r(Y) patients, (2) the late replication of some of the small r(X) chromosomes associated with this phenotype, and (3) the expression of XIST in some of the affected patients.
Assuntos
Mosaicismo , RNA não Traduzido , Cromossomos em Anel , Síndrome de Turner/genética , Mecanismo Genético de Compensação de Dose , Feminino , Humanos , Lactente , Recém-Nascido , Deficiência Intelectual/genética , Fenótipo , Fisiognomia , RNA Longo não Codificante , Fatores de Transcrição/biossíntese , Síndrome de Turner/patologiaRESUMO
We recently began a cytogenetic and molecular study of nondisjunction in leukemic Down syndrome individuals to determine whether the mechanism by which the extra chromosome 21 originates predisposes the individual to leukemia. In the present report, we summarize our observations on 18 patients with trisomy 21 and acute or transient leukemia, including 11 patients with acute lymphocytic leukemia, three with acute myeloid leukemia, one with B-cell lymphoma, one with acute megakaryoblastic leukemia, and two with transient leukemia. Results of DNA marker studies of the parental origin of the extra chromosome 21 indicated that 16 of the 18 cases (89%) were maternally derived, a percentage similar to that seen among nonleukemic Down syndrome patients. We noted that most leukemic Down syndrome patients had one locus or more in which parental heterozygosity was maintained in the trisomic individual, indicating a meiotic rather than a mitotic origin for the trisomy.
Assuntos
Síndrome de Down/genética , Leucemia/genética , Não Disjunção Genética , Adolescente , Criança , Pré-Escolar , Síndrome de Down/complicações , Marcadores Genéticos , Humanos , Lactente , Recém-Nascido , Cariotipagem , Leucemia/complicações , Recombinação GenéticaRESUMO
To assess the association between recombination and nondisjunction of chromosome 21, we analyzed cytogenetic and DNA markers in 104 trisomy 21 individuals and their parents. Our DNA marker studies of parental origin were informative in 100 cases, with the overwhelming majority (94) being maternal in origin. This value is significantly higher than the 75%-80% maternal nondisjunction rate typically observed in cytogenetic studies of trisomy 21 and illustrates the increased accuracy of the molecular approach. Using the maternally derived cases and probing at 19 polymorphic sites on chromosome 21, we created a genetic map that spans most of the long arm of chromosome 21. The map was significantly shorter than the normal female linkage map, indicating that absence of pairing and/or recombination contributes to nondisjunction in a substantial proportion of cases of trisomy 21.
Assuntos
Cromossomos Humanos Par 21 , Síndrome de Down/genética , Não Disjunção Genética , Recombinação Genética/genética , Adulto , Mapeamento Cromossômico , Troca Genética/genética , Síndrome de Down/etiologia , Feminino , Marcadores Genéticos/genética , Humanos , Masculino , Idade MaternaRESUMO
The results of a cytogenetic and molecular reinvestigation of a series of 52 patients with Turner's syndrome are reported. No evidence of Y chromosome material was found among the patients with a 45,X constitution but two patients were found to have a cell line with a r(Y) chromosome which was previously thought to be a r(X). The parental origin of the single X in the 45,X patients was maternal in 69% and paternal in 31%, a similar ratio to that seen among spontaneously aborted 45,X conceptuses. This suggests that X-chromosome imprinting is not responsible for the two grossly different phenotypes associated with a 45,X chromosome constitution. Approximately half of the structurally abnormal X chromosomes were maternal in origin and half paternal. This observation is consistent with either a meiotic or post-zygotic mitotic origin and at variance with the predominantly paternal origin reported for autosome structural abnormalities.