Lilia C. Marín Padrón

Lilia C. Marín Padrón

Auto-generated profile, based on publicly available information

Lilia C. Marín Padrón

Centro Nacional de Genética Médica, Laboratorio de Genética Bioquímica. La Habana, Cuba

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
16 May 2022 in MEDICC Review
Verified
Journal Article
Open access
NPNayade Pereira-Roche
Nayade Pereira-Roche
HRHilda Roblejo
Hilda Roblejo
LMLilia C. Marín-Padrón
Lilia C. Marín-Padrón
RIRodolfo Izaguirre-Rodríguez
Rodolfo Izaguirre-Rodríguez
Francisco Sotomayor-LugoFrancisco Sotomayor-Lugo
Francisco Sotomayor-Lugo
BMBeatriz Marcheco-Teruel
Beatriz Marcheco-Teruel
INTRODUCTION COVID-19 sequelae, or the short-, medium-, and long-term manifestations of the disease are under continuous study. There are currently few reports on the evolution of hematological variables following a demonstrated absence of SARS-CoV-2 after infection. OBJECTIVE Identify hematological alterations in Cuban adults recovered from SARS-CoV-2 infection, and their relation with disease severity. METHODS We […]

5 January 2025 in SCT Proceedings in Interdisciplinary Insights and Innovations
Verified
Journal Article
Open access
PDF file
JCJessica Laura Páez Campos
Jessica Laura Páez Campos
GFGretel Riverón Forment
Gretel Riverón Forment
TSTatiana Acosta Sánchez
Tatiana Acosta Sánchez
LRLaritza Martínez Rey
Laritza Martínez Rey
LPLilia C. Marín Padrón
Lilia C. Marín Padrón
GPGrettel Huertas Pérez
Grettel Huertas Pérez
Introduction: aminoacidopathies are a group of inborn errors of metabolism caused by defects in metabolic pathways involving amino acids. Quantification of serum amino acids is necessary for the diagnosis of these defects.Objective: to analized the serum amino acid profile in patients with clinical manifestations of aminoacidopathies.Methods: an observational, descriptive, prospective case series study was carried out. 32 pediatric patients of both sexes with clinical manifestation of aminoacidopathies from 9 provinces of the country treated in specialized Clinical Genetics clinics were included. The samples were sent to the Biochemical Genetics Laboratory of the National Center for Medical Genetics in the period between January 2023 and June 2024. Ten serum amino acids were quantified by a High-Performance Reverse-Phase Liquid Chromatography method and pre-column derivatization with o-phthaldehyde implemented in the Laboratory.Results: in the sample studied, the male sex predominated and the largest number of cases was contributed by the province of Havana. 53 % of the patients corresponded to the age group of 1 to 6 years. Neurological alterations and metabolic acidosis were the mains reasons for requesting a serum aminogram. In 59 % of the cases (19/32), significant alterations in the amino acid profile were identified, which allowed the identification of several types of aminoacidopathies as a possible diagnosis of the cases studied.Conclusions: the analysis of the serum amino acid profile is essential for the diagnosis of aminoacidopathies in patients with clinical alterations suggestive of these entities