Asunto(s)
Enfermedades del Desarrollo Óseo/genética , Luxación Congénita de la Cadera/genética , Cadera/anomalías , Isquion/anomalías , Rótula/anomalías , Proteínas de Dominio T Box/genética , Adolescente , Adulto , Enfermedades del Desarrollo Óseo/complicaciones , Enfermedades del Desarrollo Óseo/epidemiología , Enfermedades del Desarrollo Óseo/fisiopatología , Niño , Preescolar , Femenino , Cadera/fisiopatología , Luxación Congénita de la Cadera/complicaciones , Luxación Congénita de la Cadera/epidemiología , Luxación Congénita de la Cadera/fisiopatología , Humanos , Isquion/fisiopatología , Masculino , Persona de Mediana Edad , Mutación , Rótula/fisiopatología , Linaje , Fenotipo , Adulto JovenRESUMEN
During limb development, the spatio-temporal expression of sonic hedgehog (SHH) is driven by the Zone of polarizing activity Regulatory Sequence (ZRS), located 1 megabase upstream from SHH. Gain-of-function mutations of this enhancer, which cause ectopic expression of SHH, are known to be responsible for congenital limb malformations with variable expressivity, ranging from preaxial polydactyly or triphalangeal thumbs to polysyndactyly, which may also be associated with mesomelic deficiency. In this report, we describe a patient affected with mirror-image polydactyly of the four extremities and bilateral tibial deficiency. The proband's father had isolated preaxial polydactyly type II (PPD2). Using Sanger sequencing, a ZRS point mutation (NC_000007.14, g.156584153A>G, UCSC, Build hg.19) was only identified in the patient. However, pyrosequencing analysis enabled the detection of a 10% somatic mosaic in the blood and saliva from the father. To our knowledge, this is the first description of a ZRS mosaic mutation. This report highlights the complexity of genotype-phenotype correlation in ZRS-associated syndromes and the importance of detecting somatic mosaicism for accurate genetic counselling.
Asunto(s)
Anomalías Múltiples/genética , Anomalías Congénitas/genética , Ectromelia/genética , Deformidades Congénitas del Pie/genética , Deformidades Congénitas de la Mano/genética , Proteínas Hedgehog/genética , Disostosis Mandibulofacial/genética , Mosaicismo , Nariz/anomalías , Mutación Puntual , Anomalías Múltiples/metabolismo , Adulto , Anomalías Congénitas/metabolismo , Análisis Mutacional de ADN , Ectromelia/metabolismo , Deformidades Congénitas del Pie/metabolismo , Deformidades Congénitas de la Mano/metabolismo , Humanos , Lactante , Recién Nacido , Masculino , Disostosis Mandibulofacial/metabolismo , Mucosa Nasal/metabolismo , LinajeRESUMEN
Nager syndrome belongs to the group of acrofacial dysostosis, which are characterized by the association of craniofacial and limb malformations. Recently, exome sequencing studies identified the SF3B4 gene as the cause of this condition in most patients. SF3B4 encodes a highly conserved protein implicated in mRNA splicing and bone morphogenic protein (BMP) signaling. We performed SF3B4 sequencing in 14 families (18 patients) whose features were suggestive of Nager syndrome and found nine mutations predicted to result in loss-of-function. SF3B4 is the major gene responsible for autosomal dominant Nager syndrome. All mutations reported predict null alleles, therefore precluding genotype-phenotype correlations. Most mutation-negative patients were phenotypically indistinguishable from patients with mutations, suggesting genetic heterogeneity.
Asunto(s)
Predisposición Genética a la Enfermedad/genética , Haploinsuficiencia/genética , Disostosis Mandibulofacial/genética , Fenotipo , Proteínas de Unión al ARN/genética , Secuencia de Bases , Femenino , Genes Dominantes/genética , Humanos , Masculino , Disostosis Mandibulofacial/patología , Datos de Secuencia Molecular , Mutación/genética , Factores de Empalme de ARN , Análisis de Secuencia de ADNRESUMEN
Split hand/foot malformation (SHFM) with long-bone deficiency (SHFLD, MIM#119100) is a rare condition characterized by SHFM associated with long-bone malformation usually involving the tibia. Previous published data reported several unrelated patients with 17p13.3 duplication and SHFLD. Recently, the minimal critical region had been reduced, suggesting that BHLHA9 copy number gains are associated with this limb defect. Here, we report on 13 new families presenting with ectrodactyly and harboring a BHLHA9 duplication.