Literature DB >> 19396024

Overgrowth syndromes:from classical to new.

Remco Visser1, Sarina G Kant, Jan M Wit, Martijn H Breuning.   

Abstract

Overgrowth syndromes are a group of growth disorders which have gained joint attention from the fields of pediatrics, endocrinology and genetics. Major progress such as the identification of genetic causes has recently enhanced the delineation of the characteristic and non-characteristic manifestations, phenotype-genotype correlations and knowledge of the underlying pathophysiological mechanisms. As a consequence, the possibilities for distinction between the different overgrowth disorders have increased. Patients with either typical or non-typical features in whom no molecular abnormalities are found, form a basis for further research. Identification of new pathogenic alterations in these patients, best exemplified by the Marfan-related syndromes, has provided further understanding of the regulatory gene network involved. In light of recent developments and as an aid to the diagnostic process, the aim of this review is to give a comprehensive overview of the clinical, molecular genetic and pathophysiological aspects of each of the classic and new overgrowth syndromes.

Entities:  

Mesh:

Year:  2009        PMID: 19396024

Source DB:  PubMed          Journal:  Pediatr Endocrinol Rev        ISSN: 1565-4753


  8 in total

1.  De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

Authors:  Johanna Schäfgen; Kirsten Cremer; Jessica Becker; Thomas Wieland; Alexander M Zink; Sarah Kim; Isabelle C Windheuser; Martina Kreiß; Stefan Aretz; Tim M Strom; Dagmar Wieczorek; Hartmut Engels
Journal:  Eur J Hum Genet       Date:  2016-07-20       Impact factor: 4.246

Review 2.  Short and tall stature: a new paradigm emerges.

Authors:  Jeffrey Baron; Lars Sävendahl; Francesco De Luca; Andrew Dauber; Moshe Phillip; Jan M Wit; Ola Nilsson
Journal:  Nat Rev Endocrinol       Date:  2015-10-06       Impact factor: 43.330

3.  Mouse model implicates GNB3 duplication in a childhood obesity syndrome.

Authors:  Ian S Goldlust; Karen E Hermetz; Lisa M Catalano; Richard T Barfield; Rebecca Cozad; Grace Wynn; Alev Cagla Ozdemir; Karen N Conneely; Jennifer G Mulle; Shikha Dharamrup; Madhuri R Hegde; Katherine H Kim; Brad Angle; Alison Colley; Amy E Webb; Erik C Thorland; Jay W Ellison; Jill A Rosenfeld; Blake C Ballif; Lisa G Shaffer; Laurie A Demmer; M Katharine Rudd
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-26       Impact factor: 11.205

4.  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

Review 5.  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

6.  Diagnostic Work-up and Follow-up in Children with Tall Stature: A Simplified Algorithm for Clinical Practice.

Authors:  Susanne E Stalman; Anke Pons; Jan M Wit; Gerdine A Kamp; Frans B Plötz
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-12

7.  Klippel-Trenaunay Syndrome with Extensive Lymphangiomas.

Authors:  Sirin Mneimneh; Ali Tabaja; Mariam Rajab
Journal:  Case Rep Pediatr       Date:  2015-10-26

8.  Simpson-Golabi-Behmel syndrome type 1 with subclinical hypothyroidism: A case report.

Authors:  Jing Zhang; Kai Mu; Haiyan Xu; Yuehua Guo; Zhijie Liu; Liling Wang; Jiahui Li; Fengjuan Zhang; Yan Kou; Xin Yuan
Journal:  Medicine (Baltimore)       Date:  2019-10       Impact factor: 1.817

  8 in total

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