Genomic analysis in Chilean patients with suspected Rett syndrome: keep a broad differential diagnosis.

Rett syndrome (RTT, MIM #312750) is a rare genetic disorder that leads to developmental regression and severe disability and is caused by pathogenic variants in the gene. The diagnosis of RTT is based on clinical features and, depending on resources and access, on molecular confirmation. There is scarce information on molecular diagnosis from patients in Latin America, mostly due to limited availability and coverage of genomic testing.

Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.

Rare diseases affect millions of people worldwide, and most have a genetic etiology. The incorporation of next-generation sequencing into clinical settings, particularly exome and genome sequencing, has resulted in an unprecedented improvement in diagnosis and discovery in the past decade. Nevertheless, these tools are unavailable in many countries, increasing health care gaps between high- and low-and-middle-income countries and prolonging the "diagnostic odyssey" for patients.

Probing gas phase catalysis by atomic metal cations with flow tube mass spectrometry.

The evolution and applications of flow tube mass spectrometry in the study of catalysis promoted by atomic metal ions are tracked from the pioneering days in Boulder, Colorado, to the construction and application of the ICP/SIFT/QqQ and ESI/qQ/SIFT/QqQ instruments at York University and the VISTA-SIFT instrument at the Air Force Research Laboratory. The physical separation of various sources of atomic metal ions from the flow tube in the latter instruments facilitates the spatial resolution of redox reactions and allows the separate measurement of the kinetics of both legs of a two-step catalytic cycle, while also allowing a view of the catalytic cycle in progress downstream in the reaction region of the flow tube. We focus on measurements on O-atom transfer and bond activation catalysis as first identified in Boulder and emphasize fundamental aspects such as the thermodynamic window of opportunity for catalysis, catalytic efficiency, and computed energy landscapes for atomic metal cation catalysis.

Relativistic Effects in the Ligation of Atomic Coinage Metal Cations with O and CH: Anomalous Formation of Relativistic Mono- and Bis-adducts with Au.

The interaction of the atomic coinage metal cations Cu, Ag, and Au with O, a weak ligand, and CH, a strong ligand, was investigated with measurements of rate coefficients of ligation and quantum-chemical computations of ligation energies with an eye on relativistic effects going down the periodic table. Strong "third row enhancements" were observed for both the rate coefficients of ligation and ligation energies with the O ligand and for the formation of both the mono- and bis-adducts of M and the monoadduct of M(CH). The computations revealed that the third-row enhancement in the ligation energy is attributable to a relativistic increase in the ligation energy.

Toward ICP-SIFT mass spectrometry and atomic cation ligation as a probe of relativistic effects-A personal journey.

The ICP-SIFT mass spectrometer at York University, a derivative of flowing afterglow (FA) and selected-ion flow tube (SIFT) mass spectrometers, has provided a powerful technique to measure the chemistry and kinetics of atomic cation-molecule reactions. Here, I focus on periodic trends in the kinetics of ligation reactions of atomic ions with small molecules. I examine trends in ammonia ligation kinetics across the first two rows of the atomic transition metal cations and their correlation with ligand bond enthalpies and ligand field stabilization energies.