Buletin de Perinatologie Nr. 1(95) 2025: Recent submissions

  • Cabac-Pogorevici, Irina; Creangă, Iuliana; Revenco, Valeriu (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Hypertrophic cardiomyopathy (HCM) is a hereditary cardiovascular pathology with a prevalence of 1:500 to 1:200, inherited in an autosomal dominant manner. The primary presentation may be sudden cardiac death, ...
  • Răilean, Gheorghe (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Relevance: In the past five years, we have observed a significant increase in the frequency of severe neurological disorders based on the age of the child. Available data indicate that clinical manifestations predominantly ...
  • Șciuca, Svetlana; Tomacinschii, Cristina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Cystic fibrosis (CF) is the most common monogenic disease in the European population, with a prevalence that varies by region: 1:1000-1800 in Europe, 1:2000-2500 in Romania and Moldova, 1:10000 in Russia, and 1:90000 ...
  • Țurcanu, Adela; Revenco, Ninel; Cumpătă, Veronica (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Actuality: Advances in the management of rare liver disease including and liver transplantation in children have allowed them to survive into adulthood with or without a native liver. Young adults with pediatric-onset liver ...
  • Palega, Daniela; Ciuhrii, Olga; Rodoman, Iulia; Eșanu, Veronica; Pîrțu, Lucia; Palii, Ina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Pulmonary hypertension (PH) is a severe condition characterized by increased pressure in the pulmonary arteries, leading to right ventricular overload and heart failure. Early diagnosis is crucial for ...
  • Ușurelu, Natalia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Rare diseases (RD) are rare, but patients with RD are numerous, and the impact on them and their families is profound and complex. In the Republic of Moldova, the National Program for Rare Diseases (NPRD) plays ...
  • Ușurelu, Dan-Cristian; Pavlovschi, Ecaterina; Boiciuc, Chiril; Blăniță, Daniela; Ușurelu, Natalia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Phenylketonuria (PKU) is an inherited metabolic disorder caused by mutations in the PAH gene, leading to phenylalanine hydroxylase (PAH) deficiency and elevated phenylalanine (Phe) levels in the blood. ...
  • Plîngău, Ecaterina; Mîță, Valentin; Lozan, Oleg; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Molecular-genetic investigations are essential for the identification of genetic factors, but access to them is limited due to variations in public health policies. The purpose of the research is to evaluate ...
  • Machedonschii, Artiom; Sacară, Victoria; Machedonschii, Alexandr; Machedonschii, Galina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Genetic diseases pose a significant challenge, particularly in cases such as channelopathies and hyperekplexia. These disorders are associated with mutations in genes and specific genomic regions, leading to ...
  • Rodoman, Iulia; Dorif, Alexandr; Palii, Ina; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by progressive muscle degeneration. Recent studies suggest that certain microRNAs (miRNAs) may serve as biomarkers for diagnosis and ...
  • Condrea, Alexandra; Railean, Gheorghe; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Neurodegenerative diseases with pediatric onset are rare conditions characterized by progressive impairment of the central nervous system, significantly impacting patients’ quality of life. Their diagnosis ...
  • Cumpătă, Veronica; Sacară, Victoria; Țurcanu, Adela (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Wilson’s disease (WD) is a rare genetic disorder with autosomal recessive inheritance. International associations recommend family screening, including the examination of first-degree relatives of the proband ...
  • Boiciuc, Chiril; Blăniță, Daniela; Huijben, Karin; Lefeber, Dirk; Ușurelu, Natalia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Congenital disorders of glycosylation (CDG) represent a group of genetic diseases affecting the synthesis and assembly of carbohydrate on protein or lipid molecules. First described in 1980 by Prof. J. Jaeken, ...
  • Dorif, Alexandr; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Short tandem repeats (STR) were once considered completely harmless genomic elements. However, it was shown that some diseases including Huntington’s disease, Friedreich ataxia and fragile X syndrome are caused ...
  • Coliban, Iulia; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disorder caused by motor neuron degeneration. As a rare disease, SMA requires specialized diagnostic approaches that combine molecular genetic techniques ...
  • Secu, Doina; Blăniță, Daniela; Ușurelu, Natalia; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Mitochondrial diseases (MD) are a group of rare, genetically inherited disorders caused by defects in mitochondrial function, particularly in oxidative phosphorylation, leading to impaired cellular energy ...
  • Sacară, Victoria; Coliban, Iulia; Secu, Doina; Dorif, Alexandr; Boiciuc, Constantin; Egorov, Vladimir (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Molecular diagnosis represents an essential frontier in modern medicine, offering promising perspectives for managing genetic and hereditary diseases. Its relevance is growing in the context of expanding ...
  • Bauchina, Alisa; Porosencov, Egor; Dolapciu, Elena; Tutueva, Tatyana; Sacara, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Papillon-Lefèvre Syndrome (PLS), a rare autosomal recessive disorder (1/1,000,000) caused by cathepsin C gene mutation with severe periodontitis following early tooth loss. Methods involved a thorough clinical evaluation ...
  • Grin, Florin; Golub, Veniamin; Sîrbu, Ion; Nacu, Viorel (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Abstract: Nonmalignant bone tumors represent a wide variety of different entities but maintain many common features. They usually affect young patients, and most can be diagnosed through imaging exams. Often asymptomatic, ...
  • Ciubotaru, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Scop: Realizarea unei analize comparative a comportamentului contraceptiv și a gradului de autonomie decizionalală a femeilor din Republica Moldova în domeniul sănătății sexuale și reproductive, pe baza datelor din ...

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