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

Frulenko I, Ostrowska I, Patalan M, Bertoli-Avella A, León NY, Pinto A, Bauer P, Leśniak A, Katuszonek D, Glińska M, Modrzejewska M, Śmigiel R, Giżewska M

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DOI: 10.3389/fendo.2026.1858779
Published: 2026
Container: Frontiers in endocrinology
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fendo.2026.1858779,
  title = {Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report.},
  author = {Frulenko I and Ostrowska I and Patalan M and Bertoli-Avella A and León NY and Pinto A and Bauer P and Leśniak A and Katuszonek D and Glińska M and Modrzejewska M and Śmigiel R and Giżewska M},
  year = {2026},
  journal = {Frontiers in endocrinology},
  doi = {10.3389/fendo.2026.1858779},
  url = {https://doi.org/10.3389/fendo.2026.1858779}
}

RIS

TY  - JOUR
TI  - Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report.
AU  - Frulenko I
AU  - Ostrowska I
AU  - Patalan M
AU  - Bertoli-Avella A
AU  - León NY
AU  - Pinto A
AU  - Bauer P
AU  - Leśniak A
AU  - Katuszonek D
AU  - Glińska M
AU  - Modrzejewska M
AU  - Śmigiel R
AU  - Giżewska M
PY  - 2026
JO  - Frontiers in endocrinology
DO  - 10.3389/fendo.2026.1858779
UR  - https://doi.org/10.3389/fendo.2026.1858779
ER  -

APA

I, F., I, O., M, P., A, B., NY, L., A, P., P, B., A, L., D, K., M, G., M, M., R, Ś., & M, G. (2026). Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2026.1858779

Source records

pubmed · retrieved 2026-09-25T18:18:33.657Z