Literature DB >> 22705997

Overgrowth syndromes.

Orla M Neylon1, George A Werther, Matthew A Sabin.   

Abstract

PURPOSE OF REVIEW: Human growth ensues from a complex interplay of physiological factors, in the wider setting of varying genetic traits and environmental influences. Intensive research in these divergent areas, and particularly in the field of genetics, continues to clarify the molecular basis of disorders which result in overgrowth, and it is therefore timely to provide a review of these findings. RECENT
FINDINGS: This article provides an overview of the factors which regulate growth, followed by a discussion of the more commonly encountered overgrowth syndromes and their genetic basis as it is understood at the current time. There is also an added focus on recently discovered genetic associations in some conditions, such as Weaver, Perlman and Proteus syndromes.
SUMMARY: New discoveries continue to be made regarding the genetic basis for many overgrowth syndromes and the development of a much needed molecular classification system for overgrowth may become possible as the interlinking functions of these genes on growth are unravelled. As there exists a wide spectrum of syndromes, disorders resulting in overgrowth can represent a diagnostic and therapeutic challenge, from those causing prenatal overgrowth with a poor prognosis to less severe genetic aberrations which are identified in later childhood or adult life.

Entities:  

Mesh:

Year:  2012        PMID: 22705997     DOI: 10.1097/MOP.0b013e3283558995

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  11 in total

Review 1.  A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing.

Authors:  Benjamin Kamien; Anne Ronan; Gemma Poke; Ingrid Sinnerbrink; Gareth Baynam; Michelle Ward; William T Gibson; Tracy Dudding-Byth; Rodney J Scott
Journal:  Mol Syndromol       Date:  2018-01-25

Review 2.  Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.

Authors:  Merel Klaassens; Deborah Morrogh; Elisabeth M Rosser; Fatima Jaffer; Maaike Vreeburg; Levinus A Bok; Tim Segboer; Martine van Belzen; Ros M Quinlivan; Ajith Kumar; Jane A Hurst; Richard H Scott
Journal:  Eur J Hum Genet       Date:  2014-08-13       Impact factor: 4.246

3.  Carpal tunnel syndrome in paediatric patients: A novel association with Kosaki overgrowth syndrome.

Authors:  Harriet Walker; Alison Foster; Trevor Cole; Andrea Jester
Journal:  JPRAS Open       Date:  2020-07-27

Review 4.  Genetic syndromes associated with overgrowth in childhood.

Authors:  Jung Min Ko
Journal:  Ann Pediatr Endocrinol Metab       Date:  2013-09-30

5.  Orthopaedic manifestations of Proteus syndrome in a child with literature update.

Authors:  Tamer Ahmed El-Sobky; Solaf M Elsayed; Dalia M E El Mikkawy
Journal:  Bone Rep       Date:  2015-09-26

6.  Proteus Syndrome with Arteriovenous Malformation.

Authors:  Ali Asilian; Atefeh Sadat Kamali; Nabet Tajmir Riahi; Neda Adibi; Fatemeh Mokhtari
Journal:  Adv Biomed Res       Date:  2017-03-07

Review 7.  Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.

Authors:  Laura Fontana; Silvia Tabano; Silvia Maitz; Patrizia Colapietro; Emanuele Garzia; Alberto Giovanni Gerli; Silvia Maria Sirchia; Monica Miozzo
Journal:  Int J Mol Sci       Date:  2021-03-26       Impact factor: 5.923

8.  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

Review 9.  Differential diagnoses of overgrowth syndromes: the most important clinical and radiological disease manifestations.

Authors:  Letícia da Silva Lacerda; Ursula David Alves; José Fernando Cardona Zanier; Dequitier Carvalho Machado; Gustavo Bittencourt Camilo; Agnaldo José Lopes
Journal:  Radiol Res Pract       Date:  2014-06-09

10.  Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T>A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma.

Authors:  Annalisa Mencarelli; Paolo Prontera; Amedea Mencarelli; Daniela Rogaia; Gabriela Stangoni; Massimiliano Cecconi; Susanna Esposito
Journal:  Int J Mol Sci       Date:  2018-10-16       Impact factor: 5.923

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