RESUMEN
Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare autosomal dominant disorder characterized by a complex dysgenesis of the eyelids and premature ovarian insufficiency. FOXL2 located at 3q22.3, encoding a forkhead transcription factor, is the only gene known to be responsible for BPES. We describe a patient diagnosed with BPES with atypical ovarian failure, characterized by normal levels of gonadotropins, who was found to have trisomy X as well as a translocation (3;11)(q22.3;q14.1). The translocation breakpoint at 3q22.3 is located upstream of the FOXL2 gene and most likely causes BPES by separating the FOXL2 transcription unit from its cis-regulatory sequences. By array analysis we detected mosaicism for the balanced and an unbalanced form of the translocation in blood cells. We propose mitotic recombination as the likely mechanism of the mosaicism formation. Mitotic recombination is a common phenomenon in human cells. Thus, we hypothesize that it may be one of the mechanisms responsible for cryptic imbalances and possible abnormal phenotypes in some carriers of balanced rearrangements.
Asunto(s)
Cromosomas Humanos Par 11 , Cromosomas Humanos Par 3 , Predisposición Genética a la Enfermedad , Mitosis , Insuficiencia Ovárica Primaria/metabolismo , Recombinación Genética , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/genética , Translocación Genética , Trisomía/genética , Adulto , Cromosomas Humanos X/genética , Femenino , Humanos , Embarazo , Aberraciones Cromosómicas SexualesRESUMEN
Interstitial deletions involving 6q11-q14 have been reported in less than 20 patients, with the breakpoints studied by G-banding alone. We report on seven patients with 6q11-q14 interstitial deletions of variable size. The breakpoints were studied by G-banding, dual-color BAC-FISH and SNP array. The results showed the molecular breakpoints differed significantly from the ones obtained from G-banding. The breakpoints studied by BAC-FISH were consistent with the ones from SNP array. Some characteristics from this cohort are consistent with previous reports, but many typical features are lacking in our patients. The cardinal features of 6q11-q14 interstitial deletions in this cohort include: umbilical hernia, hypotonia, short stature, characteristic facial features of upslanting palpebral fissures, low set and/or dysplastic ears, high arched palate, urinary tract anomalies, and skeletal/limb anomalies.
Asunto(s)
Rotura Cromosómica , Mapeo Cromosómico/métodos , Cromosomas Humanos Par 6 , Eliminación de Secuencia , Adulto , Bandeo Cromosómico , Cromosomas Artificiales Bacterianos , Estudios de Cohortes , Cara/anomalías , Femenino , Hernia Umbilical/genética , Humanos , Hibridación Fluorescente in Situ , Recién Nacido , Cariotipificación , Masculino , Hipotonía Muscular/genética , Linaje , Polimorfismo de Nucleótido Simple , Embarazo , Nacimiento Prematuro , Adulto JovenAsunto(s)
Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Deleción Cromosómica , Cromosomas Humanos Par 6/genética , Obesidad/genética , Proteínas Represoras/genética , Anomalías Múltiples/genética , Niño , Discapacidades del Desarrollo/genética , Diagnóstico Diferencial , Femenino , Eliminación de Gen , Humanos , Hibridación Fluorescente in Situ , Fenotipo , Síndrome de Prader-Willi/genéticaRESUMEN
We report on a 6-year-old boy referred for cytogenetics study. A few non-specific features were observed in the newborn: hypotonia, failure to thrive, seizures, pre-auricular skin tags. Cat-like cry was not identified. No remarkable facial dysmorphism, gastrointestinal, respiratory or cardiac abnormalities were identified. At age 4 years, speech and motor skill delays were apparent. Karyotyping and FISH analysis revealed a de novo rearranged chromosome 5p, with subtelomeric deletion of 5p and a duplication of the cri-du-chat critical region. Array CGH using sub-megabase resolution tiling-set (SMRT) array followed by FISH analysis with labeled BACs showed a deletion of 5pter to 5p15.31 (0-6.9 Mb) and an inverted duplication of the greater part of 5p15.31 to the distal end of 5p14.3 (6.9-19.9 Mb). Although very rare, inverted duplications with terminal deletion (inv dup del) have been reported at different chromosomal ends. Our finding adds a second patient of inv dup del 5p to this growing list, and the potential causative mechanisms for this rearrangement are discussed. Review of the mapping information of cri-du-chat patients and the comparison with a previously reported patient suggested that the critical region for cat-like cry is located within a 0.6 Mb region.
Asunto(s)
Aberraciones Cromosómicas , Deleción Cromosómica , Inversión Cromosómica , Cromosomas Humanos Par 5/genética , Niño , Cromosomas Artificiales Bacterianos , Anomalías Craneofaciales/genética , Síndrome del Maullido del Gato/genética , Discapacidades del Desarrollo/genética , Genotipo , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Masculino , FenotipoRESUMEN
Distal 5q-trisomy has been reported in less than 30 patients, with craniosynostosis present in five. We report two new patients with distal 5q-trisomy craniosynostosis. Patient 1 had mild Kleeblattschädel with synostosis of multiple sutures together with wide and medially deviated thumbs and halluces, indicative of Pfeiffer syndrome. Cytogenetic and CGH analyses showed a karyotype of 46,XY,der(10)t(5;10)(q33;q26.3). Patient 2 had a prominent forehead and ridging of the metopic suture. Craniosynostosis of the metopic suture was shown by CT scan. Cytogenetic and CGH analyses disclosed a karyotype of 46,XX,der(17)t(5;17)(q35.1;p13.3). Of the 22 previously reported patients, all had microcephaly and 14 had an abnormal skull shape. Our results support the previous finding that distal 5q-trisomy together with an extra copy of the MSX2 gene leads to abnormal closure of sutures and craniosynostosis.
Asunto(s)
Cromosomas Humanos Par 5 , Craneosinostosis/diagnóstico , Craneosinostosis/genética , Proteínas de Unión al ADN/genética , Proteínas de Homeodominio/genética , Trisomía , Bandeo Cromosómico , Facies , Femenino , Humanos , Hibridación Fluorescente in Situ , Lactante , Cariotipificación , Masculino , Microcefalia/diagnóstico , Microcefalia/genética , Hibridación de Ácido NucleicoRESUMEN
Mutations in SCO2, a metallochaperone involved in mitochondrial copper delivery, are associated with early onset, fatal hypertrophic cardiomyopathy. All reported patients carry at least one copy of the common 1541G>A (E140K) mutation. Whereas patients with one copy of the E140K allele, in combination with a more deleterious mutation, follow a severe clinical course, patients homozygous for the E140K mutation have a delayed onset of disease and a more prolonged survival. Here, we have investigated a patient who appeared homozygous for the common 1541G>A mutation based on DNA sequencing and restriction enzyme analysis of a PCR product, yet presented with early onset, severe cardiomyopathy. Restriction enzyme analysis of parental DNA revealed that the mother was heterozygous for 1541G>A, while the father was homozygous wild-type. The patient showed biparental inheritance for microsatellite markers spanning the length of chromosome 22, making isodisomy unlikely. Sequencing of several single nucleotide polymorphisms within the 5'-UTR, intron and single exon of the SCO2 gene was uninformative; however, a 16 bp deletion within the intron was present in the patient and the mother, but not the father. Restriction enzyme analysis confirmed that the mother was heterozygous and that the patient was hemizygous for the deletion. Southern blot, Northern blot, and FISH analyses were consistent with the de novo deletion of one allele of SCO2 in the patient. This is the first report of hemizygosity in a SCO2 patient. The patient phenotype underscores the strikingly similar clinical course in all patients with one copy of the E140K allele. Examination of both patient and parental genotypes by thorough molecular analyses can reveal information with important implications for genetic counseling.