RESUMEN
BACKGROUND: Congenital heart disease (CHD) is one common birth malformation, accounting for â¼30% of total congenital abnormalities. AIM: Considering the unknown role of consanguinity in causing CHD, this study hypothesised that consanguineous unions and/or familial aggregation may be frequent in the Azorean Island of São Miguel (Portugal). To that end, a retrospective observational study was performed based on genealogical and molecular analyses. SUBJECTS AND METHODS: The study enrolled 112 CHD patients from São Miguel Island, which allowed the assessment of type of family (simplex or multiplex), parental consanguinity and grandparental endogamy. Based on 15 STR markers, inbreeding coefficients (FIS) in the CHD cohort and healthy control group (n = 114) were estimated. RESULTS: Multiplex families were 37.6% (n = 41/109), a rate considerably higher than previously described in the literature (< 15%). Moreover, 9.2% (n = 10/109) of the CHD families were consanguineous, mostly derived from third cousin unions, and 20.2% (n = 22/109) presented full grandparental endogamy. Higher FIS values were found in patients with parental consanguinity (0.0371) and patent ductus arteriosus (0.0277). CONCLUSION: This study analysed several genealogical and genetic features related with CHD, revealing the presence of parental consanguinity and extensive familial aggregation in the CHD patients from São Miguel Island.
Asunto(s)
Genealogía y Heráldica , Cardiopatías Congénitas/genética , Azores , Estudios de Casos y Controles , Estudios de Cohortes , Consanguinidad , Familia , Femenino , Variación Genética , Abuelos , Heterocigoto , Humanos , Desequilibrio de Ligamiento/genética , Masculino , Repeticiones de Microsatélite/genética , Padres , PortugalRESUMEN
BACKGROUND: The rearrangements of the 22q11.2 chromosomal region, most frequently deletions and duplications, have been known to be responsible for multiple congenital anomaly disorders. These rearrangements are implicated in syndromes that have some phenotypic resemblances. While the 22q11.2 deletion, also known as DiGeorge/Velocardiofacial syndrome, has common features that include cardiac abnormalities, thymic hypoplasia, characteristic face, hypocalcemia, cognitive delay, palatal defects, velopharyngeal insufficiency, and other malformations, the microduplication syndrome is largely undetected. This is mainly because phenotypic appearance is variable, milder, less characteristic and unpredictable. In this paper, we report the clinical evaluation and follow-up of two patients affected by 22q11.2 rearrangements, emphasizing new phenotypic features associated with duplication and triplication of this genomic region. CASE PRESENTATION: Patient 1 is a 24 year-old female with 22q11.2 duplication who has a heart defect (ostium secundum atrial septal defect) and supernumerary teeth (hyperdontia), a feature previously not reported in patients with 22q11.2 microduplication syndrome. Her monozygotic twin sister, who died at the age of one month, had a different heart defect (truncus arteriousus). Patient 2 is a 20 year-old female with a 22q11.2 triplication who had a father with 22q11.2 duplication. In comparison to the first case reported in the literature, she has an aggravated phenotype characterized by heart defects (restrictive VSD and membranous subaortic stenosis), and presented other facial dysmorphisms and urogenital malformations (ovarian cyst). Additionally, she has a hemangioma planum on the right side of her face, a feature of Sturge-Weber syndrome. CONCLUSIONS: In this report, we described hyperdontia as a new feature of 22q11.2 microdeletion syndrome. Moreover, this syndrome was diagnosed in a patient who had a deceased monozygotic twin affected with a different heart defect, which corresponds to a phenotypic discordance never reported in the literature. Case 2 is the second clinical report of 22q11.2 triplication and presents an aggravated phenotype in contrast to the patient previously reported.
Asunto(s)
Anomalías Múltiples/diagnóstico , Anomalías Múltiples/genética , Aberraciones Cromosómicas , Duplicación Cromosómica/genética , Síndrome de DiGeorge/diagnóstico , Síndrome de DiGeorge/genética , Diente Supernumerario/diagnóstico , Diente Supernumerario/genética , Cromosomas Humanos Par 22/genética , Facies , Femenino , Cardiopatías Congénitas/diagnóstico , Cardiopatías Congénitas/genética , Humanos , Quistes Ováricos/diagnóstico , Quistes Ováricos/genética , Fenotipo , Gemelos Monocigóticos , Adulto JovenRESUMEN
BACKGROUND: The rearrangements in the 22q11.2 chromosomal region, responsible for the 22q11.2 deletion and microduplication syndromes, are frequently associated with congenital heart disease (CHD). The present work aimed to identify the genetic basis of CHD in 87 patients from the São Miguel Island, Azores, through the detection of copy number variants (CNVs) in the 22q11.2 region. These structural variants were searched using multiplex ligation-dependent probe amplification (MLPA). In patients with CNVs, we additionally performed fluorescent in situ hybridization (FISH) for the assessment of the exact number of 22q11.2 copies among each chromosome, and array comparative genomic hybridization (array-CGH) for the determination of the exact length of CNVs. RESULTS: We found that four patients (4.6%; A to D) carried CNVs. Patients A and D, both affected with a ventricular septal defect, carried a de novo 2.5 Mb deletion of the 22q11.2 region, which was probably originated by inter-chromosomal (inter-chromatid) non-allelic homologous recombination (NAHR) events in the regions containing low-copy repeats (LCRs). Patient C, with an atrial septal defect, carried a de novo 2.5 Mb duplication of 22q11.2 region, which could have been probably generated during gametogenesis by NAHR or by unequal crossing-over; additionally, this patient presented a benign 288 Kb duplication, which included the TOP3B gene inherited from her healthy mother. Finally, patient B showed a 3 Mb triplication associated with dysmorphic facial features, cognitive deficit and heart defects, a clinical feature not reported in the only case described so far in the literature. The evaluation of patient B's parents revealed a 2.5 Mb duplication in her father, suggesting a paternal inheritance with an extra copy. CONCLUSIONS: This report allowed the identification of rare deletion and microduplication syndromes in Azorean CHD patients. Moreover, we report the second patient with a 22q11.2 triplication, and we suggest that patients with triplications of chromosome 22q11.2, although they share some characteristic features with the deletion and microduplication syndromes, present a more severe phenotype probably due to the major dosage of implicated genes.
Asunto(s)
Cromosomas Humanos Par 22/genética , Variaciones en el Número de Copia de ADN , Cardiopatías Congénitas/genética , Adolescente , Azores , Niño , Hibridación Genómica Comparativa , Femenino , Pruebas Genéticas , Humanos , Masculino , Persona de Mediana Edad , Trisomía , Adulto JovenRESUMEN
We describe 66 ciprofloxacin-nonsusceptible Streptococcus pyogenes isolates recovered from colonized and infected children. The ParC S79A substitution was frequent and associated with the emm6/sequence type 382 (emm6/ST382) lineage. The ParC D83G substitution was detected in two isolates (emm5/ST99 and emm28/ST52 lineages). One isolate (emm89/ST101) had no quinolone resistance-determining region codon substitutions or other resistance mechanisms. Five of 66 isolates were levofloxacin resistant. Although fluoroquinolones are not used in children, they may be putative disseminators of fluoroquinolone-nonsusceptible strains in the community.
Asunto(s)
Antibacterianos/farmacología , Ciprofloxacina/farmacología , Infecciones Estreptocócicas/tratamiento farmacológico , Infecciones Estreptocócicas/microbiología , Streptococcus pyogenes/efectos de los fármacos , Streptococcus pyogenes/aislamiento & purificación , Sustitución de Aminoácidos , Antígenos Bacterianos/genética , Proteínas de la Membrana Bacteriana Externa/genética , Técnicas de Tipificación Bacteriana , Proteínas Portadoras/genética , Niño , Farmacorresistencia Bacteriana/genética , Humanos , Epidemiología Molecular , Norfloxacino/farmacología , Mutación Puntual , Portugal/epidemiología , Infecciones Estreptocócicas/epidemiología , Streptococcus pyogenes/clasificación , Streptococcus pyogenes/genéticaAsunto(s)
Amnios , Enfermedades de la Córnea/patología , Enfermedades de la Córnea/cirugía , Epitelio Corneal/citología , Preservación Biológica/métodos , Trasplante de Células Madre , Células Madre , Adulto , Animales , Ciclo Celular , Diferenciación Celular , División Celular , Técnicas de Cultivo , Femenino , Humanos , Masculino , Persona de Mediana Edad , ConejosRESUMEN
During 2000-2007 in Lisbon, we identified 45 bacitracin-resistant Streptococcus pyogenes isolates among 1629 isolates: 24 from oropharyngeal healthy carriers (out of 1026), 21 from patients with noninvasive infections (out of 559) and zero from invasive infections (out of 44). Forty-four of those isolates, mainly of colonization, are low-level bacitracin-resistant members of the cMLS(B)-macrolide-resistant and tetracycline-susceptible emm28/ST52 clone previously detected in Europe, but only among clinical samples. One high-level bacitracin-resistant isolate, associated with a tonsillitis/pharyngitis episode, is cMLS(B)-macrolide-resistant and tetracycline-resistant member of the emm74/ST120 lineage, which was not previously known to include bacitracin-resistant isolates. The bcrABDR operon encoding an ATP-binding cassette transporter in Enterococcus faecalis was not detected among these bacitracin-resistant S. pyogenes strains. Virulence profiling indicated that genes coding for exotoxins and superantigens seem to be clone specific. This study provides an increased knowledge about specific bacitracin-resistant S. pyogenes strains, which may be useful in future investigations aiming to understand the mechanism(s) leading to bacitracin resistance and the cause(s) for differences in colonization and/or dissemination potential.
Asunto(s)
Antibacterianos/farmacología , Bacitracina/farmacología , Técnicas de Tipificación Bacteriana , Farmacorresistencia Bacteriana , Orofaringe/microbiología , Infecciones Estreptocócicas/microbiología , Streptococcus pyogenes/clasificación , Streptococcus pyogenes/efectos de los fármacos , Proteínas Bacterianas/genética , Portador Sano/microbiología , Análisis por Conglomerados , Dermatoglifia del ADN , Electroforesis en Gel de Campo Pulsado , Genotipo , Humanos , Lincosamidas/farmacología , Macrólidos/farmacología , Faringitis/microbiología , Portugal , Streptococcus pyogenes/genética , Streptococcus pyogenes/aislamiento & purificación , Estreptogramina B/farmacología , Tonsilitis/microbiología , Factores de Virulencia/genéticaRESUMEN
Foram analisadas cirurgias de transplante penetrante de córnea em crianças com idade de três meses a quatorze anos, realizadas no Instituto de Olhos de Goiânia nos últimos anos. Este estudo mostrou nítida diferença de resultados obtidos entre crianças na faixa etária até dez anos e nos maiores de dez. Ocorreram maiores complicaçöes no primeiro grupo, comprometendo o sucesso da intervençäo. A seleçäo dos casos foi obrigatória, näo levando à cirurgia daqueles sem perspectiva de resultados funcionais. Das vinte e seis cirurgias, quinze (57,69 por cento) obtiveram sucesso (transplante plenamente transparente). Destas quinze, treze (86,66 por cento) ficaram com acuidade visual de 20/20 a 20/40. Os outros dois (13,33 por cento) com 20/50 e 20/200. O acompanhamento destes pacientes foi de vinte meses a onze anos
Asunto(s)
Humanos , Niño , Lactante , Recién Nacido , Preescolar , Queratoplastia Penetrante/rehabilitación , Trasplante de Córnea/rehabilitaciónRESUMEN
A superfície ocular é revestida pelo epitélio corneano, límbico e conjuntival, cada um com um fenótipo celular distinto. A conjuntiva reveste as superfícies internas das pálpebras superior e inferior, e cobre a esclera anterior antes de terminar no epitélio do limbo, que é a transiçäo entre os epitélios corneano e conjuntival. O epitélio corneano, juntamente com filme lacrimal contribuem para a manutençäo da superfície opticamente regular da córnea, promovendo uma visäo nítida e adequada. Para assegurar uma superfície ocular íntegra é necessário que esta esteja constantemente coberta por um filme lacrimal estável. Recentemente, cinco importantes conceitos foram relatados para explicar como um sistema de defesa eficaz e organizado é estabelecido para se atingir este objetivo: 1) O bom estado da superfície ocular é assegurado por uma estreita relaçäo entre o epitélio da superfície ocular e o filme lacrimal; 2) A estabilidade do filme lacrimal é mantida por anexos externos; 3) O mecanismo de proteçäo em sua íntegra é controlado por uma integraçäo neuroanatômica eficaz; 4) As células germinativas (CG) epiteliais corneanas estäo localizadas no limbo; 5) A funçäo das células epiteliais da superfície ocular é mantida pela matriz e por fibroblastos do estroma.