Literature DB >> 6093533

The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.

G Neri, M E Martini-Neri, B E Katz, J M Opitz.   

Abstract

We describe a familial syndrome of renal dysplasia, Wilms tumor, hyperplasia of the endocrine pancreas, fetal gigantism, multiple congenital anomalies and mental retardation. This condition was previously described by Perlman et al [1973, 1975] and we propose to call it the "Perlman syndrome." It appears to be transmitted as an autosomal recessive trait. The possible relationships between dysplasia, neoplasia and malformation are discussed.

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Year:  1984        PMID: 6093533     DOI: 10.1002/ajmg.1320190120

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  11 in total

Review 1.  renal tumors and tumor-like lesions in pediatric patients.

Authors:  J M Kissane; L P Dehner
Journal:  Pediatr Nephrol       Date:  1992-07       Impact factor: 3.714

2.  A new lethal syndrome of exomphalos, short limbs, and macrogonadism.

Authors:  L Faivre; A L Delezoide; F Narcy; F Razavi; R Bouvier; V Cormier-Daire; M L Briard; S Lyonnet; M Vekemans; A Munnich; M Le Merrer
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

3.  Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.

Authors:  Dewi Astuti; Mark R Morris; Wendy N Cooper; Raymond H J Staals; Naomi C Wake; Graham A Fews; Harmeet Gill; Dean Gentle; Salwati Shuib; Christopher J Ricketts; Trevor Cole; Anthonie J van Essen; Richard A van Lingen; Giovanni Neri; John M Opitz; Patrick Rump; Irene Stolte-Dijkstra; Ferenc Müller; Ger J M Pruijn; Farida Latif; Eamonn R Maher
Journal:  Nat Genet       Date:  2012-02-05       Impact factor: 38.330

Review 4.  Overgrowth Syndromes.

Authors:  Andrew C Edmondson; Jennifer M Kalish
Journal:  J Pediatr Genet       Date:  2015-09-25

Review 5.  Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.

Authors:  R H Scott; C A Stiller; L Walker; N Rahman
Journal:  J Med Genet       Date:  2006-05-11       Impact factor: 6.318

6.  Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness.

Authors:  S Eggers; M R Passos-Bueno; M Zatz
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

7.  Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour.

Authors:  R G Grundy; J Pritchard; M Baraitser; A Risdon; M Robards
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

Review 8.  Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.

Authors:  Jennifer M Kalish; Leslie Doros; Lee J Helman; Raoul C Hennekam; Roland P Kuiper; Saskia M Maas; Eamonn R Maher; Kim E Nichols; Sharon E Plon; Christopher C Porter; Surya Rednam; Kris Ann P Schultz; Lisa J States; Gail E Tomlinson; Kristin Zelley; Todd E Druley
Journal:  Clin Cancer Res       Date:  2017-07-01       Impact factor: 12.531

9.  Small cell lung carcinoma in a patient with Sotos syndrome: are genes at 3p21 involved in both conditions?

Authors:  T R Cole; H E Hughes; M J Jeffreys; G T Williams; M M Arnold
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

Review 10.  Overgrowth syndromes - clinical and molecular aspects and tumour risk.

Authors:  Frédéric Brioude; Annick Toutain; Eloise Giabicani; Edouard Cottereau; Valérie Cormier-Daire; Irene Netchine
Journal:  Nat Rev Endocrinol       Date:  2019-05       Impact factor: 43.330

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