Literature DB >> 29593474

A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing.

Benjamin Kamien1,2,3, Anne Ronan1,2, Gemma Poke4, Ingrid Sinnerbrink5,6, Gareth Baynam7,8,9,10,11,12,13, Michelle Ward7, William T Gibson14,15, Tracy Dudding-Byth1,16,2,17, Rodney J Scott3,18.   

Abstract

The overgrowth syndromes are important to diagnose, not just for accurate genetic counseling, but also for knowledge surrounding cancer surveillance and prognosis. There has been a recent expansion in the number of genes associated with a mendelian overgrowth phenotype, so this review updates previous classifications of overgrowth syndromes. We also describe a clinical and molecular approach to the investigation of individuals presenting with overgrowth. This review aims to assist the clinical diagnosis of generalized overgrowth syndromes by outlining the salient features of well-known overgrowth syndromes alongside the many syndromes that have been discovered and classified more recently. We provide key clinical "handles" to aid clinical diagnosis and a list of genes to aid with panel design when using next generation sequencing, which we believe is frequently needed due to the overlapping phenotypic features seen between overgrowth syndromes.

Entities:  

Keywords:  Large stature; Macrocephaly; Macrosomia; Obesity; Overgrowth; Tall stature

Year:  2018        PMID: 29593474      PMCID: PMC5836217          DOI: 10.1159/000484532

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  100 in total

1.  Expansion of the phenotype of Kosaki overgrowth syndrome.

Authors:  Mari Minatogawa; Toshiki Takenouchi; Yu Tsuyusaki; Fuminori Iwasaki; Tomoko Uehara; Kenji Kurosawa; Kenjiro Kosaki; Cynthia J Curry
Journal:  Am J Med Genet A       Date:  2017-06-22       Impact factor: 2.802

2.  Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes.

Authors:  Christian P Kratz; Suthee Rapisuwon; Helen Reed; Henrik Hasle; Philip S Rosenberg
Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-04-15       Impact factor: 3.908

3.  A splice site mutation in HERC1 leads to syndromic intellectual disability with macrocephaly and facial dysmorphism: Further delineation of the phenotypic spectrum.

Authors:  Shagun Aggarwal; Aneek Das Bhowmik; Vedam L Ramprasad; Sakthivel Murugan; Ashwin Dalal
Journal:  Am J Med Genet A       Date:  2016-04-25       Impact factor: 2.802

4.  Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups.

Authors:  Saskia M Maas; Fleur Vansenne; Daniel J M Kadouch; Abdulla Ibrahim; Jet Bliek; Saskia Hopman; Marcel M Mannens; Johannes H M Merks; Eamonn R Maher; Raoul C Hennekam
Journal:  Am J Med Genet A       Date:  2016-07-15       Impact factor: 2.802

5.  Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation.

Authors:  Giampaolo Trivellin; Adrian F Daly; Fabio R Faucz; Bo Yuan; Liliya Rostomyan; Darwin O Larco; Marie Helene Schernthaner-Reiter; Eva Szarek; Letícia F Leal; Jean-Hubert Caberg; Emilie Castermans; Chiara Villa; Aggeliki Dimopoulos; Prashant Chittiboina; Paraskevi Xekouki; Nalini Shah; Daniel Metzger; Philippe A Lysy; Emanuele Ferrante; Natalia Strebkova; Nadia Mazerkina; Maria Chiara Zatelli; Maya Lodish; Anelia Horvath; Rodrigo Bertollo de Alexandre; Allison D Manning; Isaac Levy; Margaret F Keil; Maria de la Luz Sierra; Leonor Palmeira; Wouter Coppieters; Michel Georges; Luciana A Naves; Mauricette Jamar; Vincent Bours; T John Wu; Catherine S Choong; Jerome Bertherat; Philippe Chanson; Peter Kamenický; William E Farrell; Anne Barlier; Martha Quezado; Ivana Bjelobaba; Stanko S Stojilkovic; Jurgen Wess; Stefano Costanzi; Pengfei Liu; James R Lupski; Albert Beckers; Constantine A Stratakis
Journal:  N Engl J Med       Date:  2014-12-03       Impact factor: 91.245

6.  15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.

Authors:  Katrina Tatton-Brown; Daniela T Pilz; Karen Helene Orstavik; Michael Patton; John C K Barber; Morag N Collinson; Vivienne K Maloney; Shuwen Huang; John A Crolla; Karen Marks; Eli Ormerod; Peter Thompson; Zafar Nawaz; Christa Lese-Martin; Susan Tomkins; Paula Waits; Nazneen Rahman; Meriel McEntagart
Journal:  Am J Med Genet A       Date:  2009-02       Impact factor: 2.802

Review 7.  Beckwith-Wiedemann syndrome in adults: observations from one family and recommendations for care.

Authors:  Kimberly J Greer; Susan J Kirkpatrick; Rosanna Weksberg; Richard M Pauli
Journal:  Am J Med Genet A       Date:  2008-07-01       Impact factor: 2.802

8.  A new overgrowth syndrome is due to mutations in RNF125.

Authors:  Jair Tenorio; Alicia Mansilla; María Valencia; Víctor Martínez-Glez; Valeria Romanelli; Pedro Arias; Nerea Castrejón; Fernando Poletta; Encarna Guillén-Navarro; Gema Gordo; Elena Mansilla; Fé García-Santiago; Isabel González-Casado; Elena Vallespín; María Palomares; María A Mori; Fernando Santos-Simarro; Sixto García-Miñaur; Luis Fernández; Rocío Mena; Sara Benito-Sanz; Ángela del Pozo; Juan Carlos Silla; Kristina Ibañez; Eduardo López-Granados; Alex Martín-Trujillo; David Montaner; Karen E Heath; Ángel Campos-Barros; Joaquín Dopazo; Julián Nevado; David Monk; Víctor L Ruiz-Pérez; Pablo Lapunzina
Journal:  Hum Mutat       Date:  2014-12       Impact factor: 4.878

9.  A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.

Authors:  Anna-Maja Molin; J Andrieux; D A Koolen; V Malan; M Carella; L Colleaux; V Cormier-Daire; A David; N de Leeuw; B Delobel; B Duban-Bedu; R Fischetto; F Flinter; S Kjaergaard; F Kok; A C Krepischi; C Le Caignec; C Mackie Ogilvie; S Maia; M Mathieu-Dramard; A Munnich; O Palumbo; F Papadia; R Pfundt; W Reardon; A Receveur; M Rio; L Ronsbro Darling; C Rosenberg; J Sá; L Vallee; C Vincent-Delorme; L Zelante; M-L Bondeson; G Annerén
Journal:  J Med Genet       Date:  2011-12-17       Impact factor: 6.318

10.  De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

Authors:  Christian Babbs; Deborah Lloyd; Alistair T Pagnamenta; Stephen R F Twigg; Joanne Green; Simon J McGowan; Ghazala Mirza; Rebecca Naples; Vikram P Sharma; Emanuela V Volpi; Veronica J Buckle; Steven A Wall; Samantha J L Knight; Jeremy R Parr; Andrew O M Wilkie
Journal:  J Med Genet       Date:  2014-09-16       Impact factor: 6.318

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  11 in total

Review 1.  Overgrowth Syndrome.

Authors:  Yahan Li; Callum G Donnelly; Rocío Melissa Rivera
Journal:  Vet Clin North Am Food Anim Pract       Date:  2019-07       Impact factor: 3.357

Review 2.  Hypoglycemia due to PI3K/AKT/mTOR signaling pathway defects: two novel cases and review of the literature.

Authors:  Evelina Maines; Roberto Franceschi; Diego Martinelli; Fiorenza Soli; Francesca Romana Lepri; Giovanni Piccoli; Massimo Soffiati
Journal:  Hormones (Athens)       Date:  2021-04-20       Impact factor: 2.885

Review 3.  Targeting Metabolic Plasticity and Flexibility Dynamics for Cancer Therapy.

Authors:  Sarah-Maria Fendt; Christian Frezza; Ayelet Erez
Journal:  Cancer Discov       Date:  2020-11-02       Impact factor: 38.272

4.  Overgrowth syndromes and pediatric cancers: how many roads lead to IGF2?

Authors:  Ruthrothaselvi Bharathavikru; Nicholas D Hastie
Journal:  Genes Dev       Date:  2018-08-01       Impact factor: 11.361

Review 5.  Tall Stature: A Challenge for Clinicians.

Authors:  Beatriz Corredor; Mehul Dattani; Chiara Gertosio; Mauro Bozzola
Journal:  Curr Pediatr Rev       Date:  2019

6.  Genetic variation associated with childhood and adult stature and risk of MYCN-amplified neuroblastoma.

Authors:  Eleanor C Semmes; Erica Shen; Jennifer L Cohen; Chenan Zhang; Qingyi Wei; Jillian H Hurst; Kyle M Walsh
Journal:  Cancer Med       Date:  2020-09-17       Impact factor: 4.452

7.  Sotos syndrome with a novel mutation in the NSD1 gene associated with congenital hypothyroidism.

Authors:  Arushi Verma; Parisa Salehi; Anne Hing; Alissa Jeanne Curda Roberts
Journal:  Int J Pediatr Adolesc Med       Date:  2020-06-26

8.  Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations.

Authors:  Hyun Jin Park; Chang Ho Shin; Won Joon Yoo; Tae-Joon Cho; Man Jin Kim; Moon-Woo Seong; Sung Sup Park; Jeong Ho Lee; Nam Suk Sim; Jung Min Ko
Journal:  Orphanet J Rare Dis       Date:  2020-08-10       Impact factor: 4.123

Review 9.  International consensus recommendations on the diagnostic work-up for malformations of cortical development.

Authors:  Renske Oegema; Tahsin Stefan Barakat; Martina Wilke; Katrien Stouffs; Dina Amrom; Eleonora Aronica; Nadia Bahi-Buisson; Valerio Conti; Andrew E Fry; Tobias Geis; David Gomez Andres; Elena Parrini; Ivana Pogledic; Edith Said; Doriette Soler; Luis M Valor; Maha S Zaki; Ghayda Mirzaa; William B Dobyns; Orly Reiner; Renzo Guerrini; Daniela T Pilz; Ute Hehr; Richard J Leventer; Anna C Jansen; Grazia M S Mancini; Nataliya Di Donato
Journal:  Nat Rev Neurol       Date:  2020-09-07       Impact factor: 42.937

Review 10.  Fetal Growth Acceleration-Current Approach to the Big Baby Issue.

Authors:  Jan Modzelewski; Anna Kajdy; Katarzyna Muzyka-Placzyńska; Dorota Sys; Michał Rabijewski
Journal:  Medicina (Kaunas)       Date:  2021-03-02       Impact factor: 2.430

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