Tag: maternal health

  • Zika

    Zika

    Explore the complexities of the Zika virus, a mosquito-borne illness with potentially severe implications, especially for pregnant women. This article covers Zika’s causes, symptoms, diagnosis, treatment options, and prevention strategies, along with personal stories that underscore its impact. Stay informed to safeguard yourself and your loved ones against this persistent public health challenge.

  • VSD

    VSD

    Explore the complexities of Ventricular Septal Defect (VSD), a common congenital heart defect characterized by an abnormal opening in the heart’s ventricular septum. Discover its causes, symptoms, and treatment options, as well as important preventive measures and the significance of early diagnosis for better health outcomes. Dive into personal stories and expert insights that shed…

  • Vaginal Birth After Cesarean (VBAC)

    Vaginal Birth After Cesarean (VBAC)

    Explore the benefits and considerations of Vaginal Birth After Cesarean (VBAC), a choice many women pursue for its potential for quicker recovery and lower maternal risks. This blog post delves into the eligibility criteria, common myths, and personal experiences, empowering expectant mothers with essential knowledge and resources for a successful VBAC journey.

  • Varicella Embryopathy

    Varicella Embryopathy

    Discover the critical insights surrounding Varicella Embryopathy, a rare condition affecting infants born to mothers who contract chickenpox during early pregnancy. This blog post delves into its causes, symptoms, and the importance of early diagnosis and intervention, while providing essential preventive measures and resources for affected families. Stay informed to better understand and manage this…

  • Turner-Varny Syndrome

    Turner-Varny Syndrome

    Explore the complexities of Turner-Varny Syndrome, a rare genetic disorder affecting both sexes, characterized by short stature, cardiac defects, and developmental delays. This blog post delves into its causes, symptoms, diagnosis, and treatment options, while also addressing common myths and offering essential support resources for affected individuals and their families.

  • Twin-to-Twin Transfusion Syndrome

    Twin-to-Twin Transfusion Syndrome

    Discover the complexities of Twin-to-Twin Transfusion Syndrome (TTTS), a serious condition affecting identical twins sharing a placenta. This blog post explores its causes, symptoms, diagnosis, and treatment options, emphasizing the importance of early intervention and support for impacted families. Gain insights into the emotional challenges faced by families and the resources available for those navigating…

  • Torch Infection

    Torch Infection: Definition and Description of Torch Infection: Torch Infection refers to a group of congenital infections that can affect a developing fetus during pregnancy. The acronym ‘TORCH’ stands for Toxoplasmosis, Other infections (such as syphilis, varicella and parvovirus), Rubella, Cytomegalovirus (CMV), and Herpes Simplex Virus (HSV). These infections can lead to severe developmental issues,…

  • TORCH Syndrome

    TORCH Syndrome: Definition and Description of TORCH Syndrome: TORCH Syndrome is a complex of congenital infections that can lead to a variety of serious health problems in newborns. The acronym “TORCH” stands for Toxoplasmosis, Other (which includes infections like syphilis), Rubella, Cytomegalovirus (CMV), and Herpes Simplex Virus (HSV). These infections are especially concerning when contracted…

  • Syphilis, Congenital

    Syphilis, Congenital: Definition and Description of Syphilis, Congenital: Congenital syphilis is a severe infectious disease that occurs when a mother passes the syphilis bacterium, Treponema pallidum, to her baby during pregnancy or childbirth. This condition can lead to a range of health issues for the newborn, including developmental delays, deformities, and in severe cases, stillbirth.…

  • RS, X-Linked

    RS, X-Linked: Definition and Description of RS, X-Linked: RS, X-Linked, commonly known as Rieger syndrome, is a genetic condition characterized by abnormalities in the development of the eyes, teeth, and other organs. This disorder is associated with mutations on the X chromosome, leading to a spectrum of developmental anomalies. Individuals with Rieger syndrome may display…