Asunto(s)
Anomalías Múltiples/genética , Agenesia del Cuerpo Calloso/genética , Proteínas de Unión al ADN/genética , Hiperqueratosis Epidermolítica/genética , Hipertricosis/genética , Discapacidad Intelectual/genética , Mutación , Factores de Transcripción/genética , Anomalías Múltiples/diagnóstico , Adolescente , Adulto , Agenesia del Cuerpo Calloso/diagnóstico , Niño , Facies , Femenino , Estudios de Asociación Genética , Humanos , Hiperqueratosis Epidermolítica/diagnóstico , Hipertricosis/diagnóstico , Discapacidad Intelectual/diagnóstico , Fenotipo , Secuenciación del Exoma , Adulto JovenRESUMEN
BACKGROUND: Using array techniques, it was recently shown that about 10% of patients with mental retardation of unknown origin harbour cryptic chromosomal aneusomies. However, data analysis is currently not standardised and little is known about its sensitivity and specificity. METHODS: We have developed an electronic data analysis tool for gene-mapping SNP arrays, a software tool that we call Copy Number Variation Finder (CNVF). Using CNVF, we analysed 104 unselected patients with mental retardation of unknown origin with a genechip mapping 100K SNP array and established an optimised set of analysis parameters. RESULTS: We detected deletions as small as 20 kb when covered by at least three single-nucleotide polymorphisms (SNPs) and duplications as small as 150 kb when covered by at least six SNPs, with only one false-positive signal in six patients. In 9.1% of patients, we detected apparently disease-causing or de novo aberrations ranging in size from 0.4 to 14 Mb. Morphological anomalies in patients with de novo aberrations were equal to that of unselected patients when measured with de Vries score. CONCLUSION: Our standardised CNVF data analysis tool is easy to use and has high sensitivity and specificity. As some genomic regions are covered more densely than others, the genome-wide resolution of the 100K array is about 400-500 kb for deletions and 900-1000 kb for duplications. The detection rate of about 10% of de novo aberrations is independent of selection of patients for particular features. The incidental finding in two patients of heterozygosity for the 250 kb recurrent deletion at the NPH1 locus, associated with autosomal recessive juvenile nephronophthisis, which was inherited from a healthy parent, highlights the fact that inherited aberrations might be disease-related even though not causal for mental retardation.
Asunto(s)
Discapacidad Intelectual/genética , Polimorfismo de Nucleótido Simple , Aberraciones Cromosómicas , Técnicas Genéticas , Variación Genética , Genoma , Heterocigoto , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Hibridación de Ácido Nucleico , Análisis de Secuencia por Matrices de Oligonucleótidos , Sensibilidad y Especificidad , Análisis de Secuencia de ADNRESUMEN
Kabuki syndrome is a rare dysmorphogenic disorder. The central nervous system is often involved, and epilepsy is a common symptom. The diagnosis is clinical, and no typical electroencephalographic findings have thus far been reported. We have documented temporo-occipital spikes in sleep electroencephalogram in all our three Kabuki patients. The location of the spikes was similar in all cases although their occurrence varied from continuous spiking to single spikes. We suggest that temporo-occipital spikes are typical in Kabuki syndrome and discuss the possible cause of this finding.
Asunto(s)
Anomalías Múltiples/fisiopatología , Electroencefalografía/métodos , Discapacidad Intelectual/fisiopatología , Lóbulo Occipital/fisiopatología , Lóbulo Temporal/fisiopatología , Adolescente , Niño , Epilepsia/complicaciones , Epilepsia/fisiopatología , Femenino , Humanos , Discapacidad Intelectual/complicaciones , Masculino , SíndromeRESUMEN
The facial photos of 76 aspartylglucosaminuria (AGU) patients, 29 obligate carriers and 78 unrelated controls were evaluated for dysmorphic features to see whether this autosomal recessive lysosomal storage disease includes a dysmorphic facial gestalt in addition to the well-known age-related coarsening of the facies and whether the carrier status of AGU might have an effect on the facial features. A consistent dysmorphic gestalt with hypertelorism, a short and broad nose with round nares, simple often small ears with small or missing lobule and modest folding of helices, thick lips and a square shape of face, was found to be present long before the coarsening begins. Recognition of this pattern of facial features might help in the early diagnosis of AGU. Statistically, puffy eyelids were found to be significantly more frequent in AGU carriers than in controls. These findings support an earlier implication that AGU carrier status might have a slight influence on the phenotype.
Asunto(s)
Aspartilglucosilaminasa/orina , Enfermedades por Almacenamiento Lisosomal/diagnóstico , Errores Innatos del Metabolismo/diagnóstico , Adolescente , Adulto , Anciano , Niño , Preescolar , Párpados , Cara , Facies , Femenino , Heterocigoto , Homocigoto , Humanos , Hipertelorismo , Enfermedades por Almacenamiento Lisosomal/patología , Masculino , Errores Innatos del Metabolismo/patología , Persona de Mediana Edad , FenotipoRESUMEN
We report three unrelated patients with hypertrichosis, mild to moderate mental retardation, and dysmorphic facial features including low anterior hairline, thick arched eyebrows, nose with broad tip and columella below alae nasi, short philtrum, thick drooping lower lip and simple posteriorly rotated ears. They also had rough skin with hyperkeratotic plaques. Feet and finger tips were broad. All of them had personality problems like aggressiveness, stubborn temperament or tendency to withdraw. Brain MRI showed thick and short corpus callosum. We believe that these patients represent a new syndrome of unknown aetiology.
Asunto(s)
Agenesia del Cuerpo Calloso , Cara/anomalías , Hipertricosis/patología , Discapacidad Intelectual/patología , Adolescente , Niño , Femenino , Humanos , Imagen por Resonancia MagnéticaRESUMEN
Pitt-Hopkins syndrome is a rarely reported syndrome of so-far-unknown etiology characterized by mental retardation, wide mouth, and intermittent hyperventilation. By molecular karyotyping with GeneChip Human Mapping 100K SNP arrays, we detected a 1.2-Mb deletion on 18q21.2 in one patient. Sequencing of the TCF4 transcription factor gene, which is contained in the deletion region, in 30 patients with significant phenotypic overlap revealed heterozygous stop, splice, and missense mutations in five further patients with severe mental retardation and remarkable facial resemblance. Thus, we establish the Pitt-Hopkins syndrome as a distinct but probably heterogeneous entity caused by autosomal dominant de novo mutations in TCF4. Because of its phenotypic overlap, Pitt-Hopkins syndrome evolves as an important differential diagnosis to Angelman and Rett syndromes. Both null and missense mutations impaired the interaction of TCF4 with ASCL1 from the PHOX-RET pathway in transactivating an E box-containing reporter construct; therefore, hyperventilation and Hirschsprung disease in patients with Pitt-Hopkins syndrome might be explained by altered development of noradrenergic derivatives.
Asunto(s)
Hiperventilación/complicaciones , Hiperventilación/genética , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/genética , Mutación , Factores de Transcripción TCF/genética , Adolescente , Adulto , Factores de Transcripción Básicos con Cremalleras de Leucinas y Motivos Hélice-Asa-Hélice , Línea Celular , Niño , Deleción Cromosómica , Cromosomas Humanos Par 18/genética , Proteínas de Unión al ADN , Cara/anomalías , Femenino , Genes Dominantes , Haplotipos , Humanos , Hibridación Fluorescente in Situ , Masculino , Fenotipo , Polimorfismo de Nucleótido Simple , Síndrome , Factor de Transcripción 4 , Proteína 2 Similar al Factor de Transcripción 7 , Factores de Transcripción , TransfecciónRESUMEN
Pitt-Hopkins syndrome is a rare dysmorphic mental retardation syndrome marked by daytime spells of overbreathing interrupted by apnoea. The dysmorphism consists of a large beaked nose, cup-shaped ears with broad helices, a wide mouth, Cupid's bow upper lip, wide and shallow palate and broad or clubbed fingertips. The four patients described so far have been sporadic and represented both sexes. In addition, a pair of sibs with atypical features has been reported as possible Pitt-Hopkins syndrome cases. We describe two unrelated Pitt-Hopkins syndrome patients in order to further define the phenotype. In addition to severe developmental retardation, hypotonia, postnatal growth retardation, microcephaly, abnormal breathing and characteristic dysmorphic features, both had epilepsy and intestinal problems with severe constipation in one and Hirschsprung disease in the other. Other abnormalities were hypopigmented skin macules in one and high-grade myopia in the other. Both had unusual frontal slow-and-sharp-wave discharges on electroencephalography. Magnetic resonance imaging in both showed a similar hypoplastic corpus callosum with missing rostrum and posterior part of the splenium and bulbous caudate nuclei bulging towards the frontal horns. Chromosomal analysis and subtelomere fluorescence in-situ hybridization studies were normal. No mutations were found in the MECP2 or ZFHX1B genes. Extensive metabolic and mitochondrial screens were normal. The electroencephalography and brain magnetic resonance imaging findings appear to be further diagnostic signs in Pitt-Hopkins syndrome, which is also one of the syndromes associated with Hirschsprung disease.