Publications by authors named "L C Marquez-Quiroz"
Article Synopsis
- Chromosomal rearrangements can alter gene expression and lead to various disorders, including neurodevelopmental delays and autism.
- A specific case of a 2-year-old boy with neurodevelopmental delay linked to a 15q24 duplication highlights the complexities in understanding the effects of such genetic changes.
- A multidisciplinary approach is recommended for evaluating conditions like autism and language delays to improve diagnosis and support for affected families.
Temple syndrome (TS14) can be originated by maternal uniparental disomy (UPD(14)mat), paternal deletion, or epimutation, leading to disturbances in 14q32.2 imprinted region. The most frequent phenotypic manifestations are prenatal and postnatal growth failure, hypotonia, developmental delay, small hands/feet, precocious puberty, and truncal obesity.
View Article and Find Full Text PDFBackground And Purpose: Myotonic Dystrophy Type I (DM1) is a neurodegenerative, genetic, and multisystemic disorder with a large variety of symptoms due to a CTG trinucleotide expansion located on Dystrophia Myotonica Protein Kinase (DMPK) gene. Previous reports have shown cognitive deterioration in these patients. Given that white matter (WM) degradation has also been reported in DM1 patients, here we explored if alterations in the cognitive profile of DM1 patients could be related to the deterioration of WM.
View Article and Find Full Text PDFIntroduction: Myotonic dystrophy type 1 (DM1) is a multisystemic disorder characterized mainly by skeletal muscle alterations. Although oropharyngeal dysphagia is a prominent clinical feature of DM1, it remains poorly studied in its early disease stages.
Methods: Dysphagia was investigated in 11 presymptomatic DM1 carriers, 14 patients with DM1 and 12 age-matched healthy controls, by using fiberoptic endoscopic evaluation of swallowing (FEES) and clinical scores.