A surviving case of papillorenal syndrome with the phenotype of Potter sequence.

doi:10.1111/j.1442-200X.2010.03261.x

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Article

A surviving case of papillorenal syndrome with the phenotype of Potter sequence.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Jun 2011

Fujioka Kazumichi, Morioka Ichiro, Nozu Kandai, Nishimoto Masashi, Amano Mariko, Tagami Mizuki, Honda Shigeru, Yokoyama Naoki, Yamada Hideto, Iijima Kazumoto, Matsuo Masafumi

Abstract excerpt

No abstract is available from the source.

Topics

Adult
Cesarean Section
Coloboma
Diagnosis, Differential
Female
Fetal Diseases
Follow-Up Studies
Humans
Infant, Newborn
Magnetic Resonance Imaging
Male
Mutation
PAX2 Transcription Factor
Phenotype
Pregnancy
Prenatal Diagnosis
Renal Insufficiency
Vesico-Ureteral Reflux

Source

Open in PubMed

Identifiers

PMID: 21696512
DOI: 10.1111/j.1442-200X.2010.03261.x

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