Literature DB >> 9863604

Costello syndrome: two cases with embryonal rhabdomyosarcoma.

B Kerr1, O B Eden, R Dandamudi, N Shannon, O Quarrell, A Emmerson, E Ladusans, M Gerrard, D Donnai.   

Abstract

Costello syndrome is a well delineated mental retardation syndrome of unknown aetiology in which the occurrence of benign tumours, especially papillomata, is recognised. We report two children in whom the diagnosis of Costello syndrome was made in the first months of life, who both developed a retroperitoneal embryonal rhabdomyosarcoma. Although not previously reported, the occurrence of this relatively uncommon childhood tumour in two girls with Costello syndrome suggests that an increased risk of malignancy may be part of this condition. The genetic basis of this susceptibility requires further clarification.

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Year:  1998        PMID: 9863604      PMCID: PMC1051519          DOI: 10.1136/jmg.35.12.1036

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  19 in total

1.  A new syndrome: mental subnormality and nasal papillomata.

Authors:  J M Costello
Journal:  Aust Paediatr J       Date:  1977-06

Review 2.  Facio-cutaneous-skeletal syndrome is the Costello syndrome.

Authors:  R A Martin; K L Jones
Journal:  Am J Med Genet       Date:  1993-08-15

Review 3.  Not a new MCA/MR syndrome but probably Costello syndrome?

Authors:  V M Der Kaloustian
Journal:  Am J Med Genet       Date:  1993-08-15

4.  International variations in the incidence of childhood soft-tissue sarcomas.

Authors:  C A Stiller; D M Parkin
Journal:  Paediatr Perinat Epidemiol       Date:  1994-01       Impact factor: 3.980

5.  Costello syndrome.

Authors:  O Dearlove; N Harper
Journal:  Paediatr Anaesth       Date:  1997       Impact factor: 2.556

6.  Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma.

Authors:  J Toguchida; T Yamaguchi; S H Dayton; R L Beauchamp; G E Herrera; K Ishizaki; T Yamamuro; P A Meyers; J B Little; M S Sasaki
Journal:  N Engl J Med       Date:  1992-05-14       Impact factor: 91.245

Review 7.  New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.

Authors:  Z Borochowitz; L Pavone; G Mazor; R Rizzo; H Dar
Journal:  Am J Med Genet       Date:  1992-07-01

8.  Report on two patients with Costello syndrome and sialuria.

Authors:  M Di Rocco; R Gatti; P Gandullia; A Barabino; P Picco; C Borrone
Journal:  Am J Med Genet       Date:  1993-11-15

Review 9.  Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.

Authors:  G Zampino; P Mastroiacovo; R Ricci; M Zollino; G Segni; M E Martini-Neri; G Neri
Journal:  Am J Med Genet       Date:  1993-08-15

10.  Costello syndrome.

Authors:  V M Der Kaloustian; B Moroz; N McIntosh; A K Watters; S Blaichman
Journal:  Am J Med Genet       Date:  1991-10-01
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  10 in total

Review 1.  High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: brain overgrowth associated with HRAS mutations as the likely cause of structural brain and spinal cord abnormalities.

Authors:  Karen W Gripp; Elizabeth Hopkins; Daniel Doyle; William B Dobyns
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

2.  Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases.

Authors:  B Kerr; M-A Delrue; S Sigaudy; R Perveen; M Marche; I Burgelin; M Stef; B Tang; O B Eden; J O'Sullivan; A De Sandre-Giovannoli; W Reardon; C Brewer; C Bennett; O Quarell; E M'Cann; D Donnai; F Stewart; R Hennekam; H Cavé; A Verloes; N Philip; D Lacombe; N Levy; B Arveiler; G Black
Journal:  J Med Genet       Date:  2006-01-27       Impact factor: 6.318

3.  Costello syndrome: Clinical phenotype, genotype, and management guidelines.

Authors:  Karen W Gripp; Lindsey A Morse; Marni Axelrad; Kathryn C Chatfield; Aaron Chidekel; William Dobyns; Daniel Doyle; Bronwyn Kerr; Angela E Lin; David D Schwartz; Barbara J Sibbles; Dawn Siegel; Suma P Shankar; David A Stevenson; Mihir M Thacker; K Nicole Weaver; Sue M White; Katherine A Rauen
Journal:  Am J Med Genet A       Date:  2019-06-20       Impact factor: 2.802

Review 4.  Dysmorphology demystified.

Authors:  William Reardon; Dian Donnai
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-05       Impact factor: 5.747

5.  Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia.

Authors:  Angela E Lin; Barbara O'Brien; Laurie A Demmer; Kristina K Almeda; Cynthia L Blanco; Patrick F Glasow; Charles I Berul; Robert Hamilton; A Micheil Innes; Julie L Lauzon; Katia Sol-Church; Karen W Gripp
Journal:  Prenat Diagn       Date:  2009-07       Impact factor: 3.050

6.  Respiratory system involvement in Costello syndrome.

Authors:  Natalia Gomez-Ospina; Christin Kuo; Amitha Lakshmi Ananth; Angela Myers; Marie-Luise Brennan; David A Stevenson; Jonathan A Bernstein; Louanne Hudgins
Journal:  Am J Med Genet A       Date:  2016-04-22       Impact factor: 2.802

7.  Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding protein.

Authors:  A Hinek; A C Smith; E M Cutiongco; J W Callahan; K W Gripp; R Weksberg
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

8.  Costello Syndrome and Umbilical Ligament Rhabdomyosarcoma in Two Pediatric Patients: Case Reports and Review of the Literature.

Authors:  Carlos Sánchez-Montenegro; Alejandra Vilanova-Sánchez; Saturnino Barrena-Delfa; Jair Tenorio; Fernando Santos-Simarro; Sixto García-Miñaur; Pablo Lapunzina; Leopoldo Martínez-Martínez
Journal:  Case Rep Genet       Date:  2017-01-19

9.  Recombinant growth hormone therapy in a girl with Costello syndrome: a 4-year observation.

Authors:  Ewa Blachowska; Elżbieta Petriczko; Anita Horodnicka-Józwa; Agata Skórka; Magdalena Pelc; Małgorzata Krajewska-Walasek; Mieczysław Walczak
Journal:  Ital J Pediatr       Date:  2016-01-26       Impact factor: 2.638

Review 10.  The impact of RASopathy-associated mutations on CNS development in mice and humans.

Authors:  Minkyung Kang; Yong-Seok Lee
Journal:  Mol Brain       Date:  2019-11-21       Impact factor: 4.041

  10 in total

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