Complex Perinatal Syndromes Affecting Early Human Growth and Development: Issues to Consider to Understand Their

Roberto Frenquelli1, Marc Ratcliff2, Jimena Villar de Onis3,4

  • 1Master Program in Child Psychoanalysis and Neuropsychological, Developmental Psychology Unit, Faculty of Psychology, National University of Rosario, Rosario, Argentina.

Insights

Complex perinatal syndromes (CPS) impact early human development. An ecological-systemic approach is crucial for understanding and intervening in these critical developmental periods to optimize long-term health outcomes.

Area of Science:

  • Perinatal health and developmental biology.
  • Human growth and developmental sciences.
  • Ecological and systemic approaches to health.

Background:

  • Complex perinatal syndromes (CPS) like preterm birth and growth restriction significantly influence lifelong health.
  • Early development involves intricate interactions between genetic, neural, and environmental factors.
  • Traditional linear models are insufficient for understanding these multifaceted developmental processes.

Purpose of the Study:

  • To advocate for an ecological-systemic approach to understand early human growth and development.
  • To highlight the need for longitudinal, interdisciplinary research in perinatal health.
  • To emphasize the importance of sensitive periods in development for intervention strategies.

Main Methods:

  • Conceptual analysis of existing research on perinatal development.
  • Advocacy for an integrated, multidimensional research framework.
  • Emphasis on longitudinal and interdisciplinary study designs.

Main Results:

  • Identified distinct fetal growth trajectories correlating with neurodevelopmental outcomes.
  • Highlighted critical postnatal windows for environmental and caregiver interactions.
  • Demonstrated the inadequacy of isolated, mechanistic interpretations of developmental influences.

Conclusions:

  • An ecological-systemic perspective is essential for a holistic understanding of CPS.
  • Interventions during sensitive developmental periods hold potential for optimizing growth and health.
  • A paradigm shift towards integrated research and clinical practice is necessary to address perinatal health challenges.

Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.9K
Nature and Nurture01:10

Nature and Nurture

Many human characteristics, like height, are shaped by both nature—in other words, by our genes—and by nurture, or our environment. For example, chronic stress during childhood inhibits the production of growth hormones and consequently reduces bone growth and height. Scientists estimate that 70-90% of variation in height is due to genetic differences among individuals, and 10-30% of variation in height is due to differences in the environments that individuals experience,...
20.9K
Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the...
42.8K
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
280
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
35.4K
Pathophysiology of Diabetes01:20

Pathophysiology of Diabetes

Diabetes mellitus is a chronic metabolic disorder characterized by hyperglycemia. The four categories of diabetes are type 1 diabetes, type 2 diabetes, other specific types of diabetes, and gestational diabetes.
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
1.3K