A case of Potter sequence with WT1 mutation

Miwa Yoshino1, Wataru Shimabukuro2,3, Mina Takeichi2

  • 1Department of Pediatrics, Kyushu Hospital, Japan Community Healthcare Organization, 1-8-1, Kishinoura, Yahatanishi-ku, Kitakyushu, Fukuoka, 806-8501, Japan. mm035m1024@yahoo.co.jp.

CEN Case Reports
|October 13, 2022
PubMed
Summary

A rare Wilms tumor 1 (WT1) gene mutation caused fetal kidney failure and Potter sequence in a neonate. This specific missense mutation may indicate severe fetal onset, highlighting the need to consider WT1 in similar cases.

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