Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report - Top-Institutions - MDSpire

Management Difficulties in a Newborn with Xp21 Contiguous Gene Deletion Syndrome: A 15-Month Case Study

  • By

  • Ignacy Frulenko

  • Iwona Ostrowska

  • Michał Patalan

  • Aida Bertoli-Avella

  • Nayla Y. León

  • Andreia Pinto

  • Peter Bauer

  • Alicja Leśniak

  • Daria Katuszonek

  • Marta Glińska

  • Monika Modrzejewska

  • Robert Śmigiel

  • Maria Giżewska

  • July 20, 2026

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Top Institutions in Pediatrics

Brief introduction explaining scope and methodology.

  • #1

    Children’s Hospital of Philadelphia
    Children’s Hospital of Philadelphia

    Philadelphia, Pennsylvania

    Key Differentiators

    • Pediatrics
    • Neonatology
    • Genetics

  • #2

    Boston Children’s Hospital
    Boston Children’s Hospital

    Boston, Massachusetts

    Key Differentiators

    • Pediatrics
    • Neonatology
    • Genetics

  • #3

    UCSF neonatal intensive care unit
    UCSF neonatal intensive care unit

    San Francisco, California

    Key Differentiators

    • Pediatrics
    • Neonatology

Original Source(s)

Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report

  • by Ignacy Frulenko, Iwona Ostrowska, Michał Patalan, Aida Bertoli-Avella, Nayla Y. León, Andreia Pinto, Peter Bauer, Alicja Leśniak, Daria Katuszonek, Marta Glińska, Monika Modrzejewska, Robert Śmigiel, Maria Giżewska

  • July 20, 2026

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