Literature DB >> 2092586

Livebirth prevalence and follow-up of malformation syndromes in 27,472 newborns.

M Higurashi1, M Oda, K Iijima, S Iijima, T Takeshita, N Watanabe, K Yoneyama.   

Abstract

The results of a survey of the birth prevalence of congenital anomalies among 27,472 consecutive newborn babies at a large maternity hospital in Tokyo are reported. There were 29 cases with trisomy-21; 5 cases with trisomy-13 syndrome; 5 with trisomy-18 syndrome; 2 with cri-du-chat syndrome; and one each with partial monosomy 4p, partial trisomy 5p, partial trisomy 6p, partial trisomy 9p, partial trisomy 9q, partial monosomy 10p, and partial monosomy 13q. Single cases of the following were observed: the Hallermann-Streiff syndrome, the Treacher-Collins syndrome, achondroplasia, arthrogryposis, the Beckwith-Wiedemann syndrome, the asplenia syndrome, the Klippel-Trenaunay-Weber syndrome, the Marfan syndrome, the Carpenter syndrome, the Goldenhar syndrome, and the Pierre Robin syndrome. The results of follow-ups to determine the life-prognosis of each patient with an autosomal aberration are reported.

Entities:  

Mesh:

Year:  1990        PMID: 2092586     DOI: 10.1016/s0387-7604(12)80004-0

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  11 in total

1.  Novel rearrangements between different chromosomes with direct impact on the diagnosis of 5p- syndrome.

Authors:  Samar Nasser Chehimi; Vanessa Tavares Almeida; Amom Mendes Nascimento; Évelin Aline Zanardo; Yanca Gasparini de Oliveira; Gleyson Francisco da Silva Carvalho; Beatriz Martins Wolff; Marilia Moreira Montenegro; Nilson Antônio de Assunção; Chong Ae Kim; Leslie Domenici Kulikowski
Journal:  Clinics (Sao Paulo)       Date:  2022-05-28       Impact factor: 2.898

2.  Educational Priorities for Children with Cri-Du-Chat Syndrome.

Authors:  Keenan A Pituch; Vanessa A Green; Robert Didden; Lisa Whittle; Mark F O'Reilly; Giulio E Lancioni; Jeff Sigafoos
Journal:  J Dev Phys Disabil       Date:  2009-11-26

Review 3.  5p deletions: Current knowledge and future directions.

Authors:  Joanne M Nguyen; Krista J Qualmann; Rebecca Okashah; AmySue Reilly; Mikhail F Alexeyev; Dennis J Campbell
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-08-03       Impact factor: 3.908

4.  Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents.

Authors:  Dilek U Alkaya; Birsen Karaman; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2020-04-02

5.  Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation.

Authors:  P C Mainardi; C Perfumo; A Calì; G Coucourde; G Pastore; S Cavani; F Zara; J Overhauser; M Pierluigi; F D Bricarelli
Journal:  J Med Genet       Date:  2001-03       Impact factor: 6.318

Review 6.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

7.  Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report.

Authors:  Yerai Vado; Javier Errea-Dorronsoro; Isabel Llano-Rivas; Nerea Gorria; Arrate Pereda; Blanca Gener; Laura Garcia-Naveda; Guiomar Perez de Nanclares
Journal:  BMC Med Genomics       Date:  2018-12-27       Impact factor: 3.063

8.  Factors Surrounding the Healthcare Transition From Pediatric to Adult Care in 5p- Syndrome: A Survey Among Healthcare Professionals.

Authors:  Yuko Ishizaki; Mari Matsuo; Kayoko Saito; Yoko Fujihira
Journal:  Front Pediatr       Date:  2022-07-08       Impact factor: 3.569

9.  Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.

Authors:  Jiasun Su; Huayu Fu; Bobo Xie; Weiliang Lu; Wei Li; Yuan Wei; Qiang Zhang; Shengkai Wei; Qiuli Chen; Yingchi Lu; Tingting Jiang; Jingsi Luo; Zailong Qin
Journal:  Mol Cytogenet       Date:  2019-12-09       Impact factor: 2.009

10.  Birth prevalence of achondroplasia: A systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Femke van Kessel; Rosa van Hoorn; Judith van den Bosch; Renée Shediac; Sarah Landis
Journal:  Am J Med Genet A       Date:  2020-08-17       Impact factor: 2.802

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.