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Updated: Aug 26, 2025

Wild-type Blocking PCR Combined with Direct Sequencing as a Highly Sensitive Method for Detection of Low-Frequency Somatic Mutations
Published on: March 29, 2017
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.
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.
Area of Science:
- Genetics
- Pediatric Nephrology
- Developmental Biology
Background:
- Wilms tumor 1 (WT1) gene mutations are linked to Denys-Drash and Frasier syndromes, typically causing kidney failure postnatally.
- Potter sequence, characterized by fetal kidney failure, often presents with distinct physical features, but this case was atypical.
- Congenital anomalies of the kidney and urinary tract (CAKUT) encompass a spectrum of developmental kidney disorders.
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