The Perlman familial nephroblastomatosis syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference18 articles.
1. Bilateral nephroblastomatosis
2. Congenital Mesoblastic Nephroma and Polyhydramnios
3. Neonatal ascites due to lysosomal storage disease.
4. Massive infantile nephroblastomatosis.A clinical, radiological, and pathological analysis of four cases
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1. DIS3L2 Gene Mutation Causes the Perlman Syndrome of Overgrowth and Wilms Tumor Susceptibility;Cureus;2023-12-01
2. Enlarged Abdominal Lymph Node as a Cause of Polyhydramnios in the Course of Congenital Neonatal Leukaemia: A Case Report and Review of the Literature on Foetal Abdominal Tumours with Coexisting Polyhydramnios;Journal of Clinical Medicine;2022-11-07
3. Ascites;Pediatric Gastrointestinal and Liver Disease;2021
4. Perinatal Tumors;The Surgery of Childhood Tumors;2016
5. Overgrowth Syndromes;Journal of Pediatric Genetics;2015-09-25
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