Literature DB >> 9571278

Goldberg-Shprintzen syndrome: report of a new family and review of the literature.

A E Fryer1.   

Abstract

In 1981, Goldberg and Shprintzen described siblings with short-segment Hirschsprung disease, cleft palate, microcephaly, mild mental retardation, short stature and distinctive facial appearance. There have been several subsequent reports which broaden the phenotype. This paper describes a further family, reviews the literature and stresses the intra-familial variability.

Entities:  

Mesh:

Year:  1998        PMID: 9571278     DOI: 10.1097/00019605-199804000-00003

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  4 in total

1.  Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features.

Authors:  K Yamada; Y Yamada; N Nomura; K Miura; R Wakako; C Hayakawa; A Matsumoto; T Kumagai; I Yoshimura; S Miyazaki; K Kato; S Sonta; H Ono; T Yamanaka; M Nagaya; N Wakamatsu
Journal:  Am J Hum Genet       Date:  2001-10-02       Impact factor: 11.025

Review 2.  Mowat-Wilson syndrome.

Authors:  D R Mowat; M J Wilson; M Goossens
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

Review 3.  The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2006-03-04       Impact factor: 1.827

4.  Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP.

Authors:  Katherine C MacKenzie; Bianca M de Graaf; Andreas Syrimis; Yuying Zhao; Erwin Brosens; Grazia M S Mancini; Rachel Schot; Dicky Halley; Martina Wilke; Arve Vøllo; Frances Flinter; Andrew Green; Sahar Mansour; Jacek Pilch; Zornitza Stark; Eleni Zamba-Papanicolaou; Violetta Christophidou-Anastasiadou; Robert M W Hofstra; Jan D H Jongbloed; Nayia Nicolaou; George A Tanteles; Alice S Brooks; Maria M Alves
Journal:  Hum Mutat       Date:  2020-09-16       Impact factor: 4.878

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.