Literature DB >> 22439039

Echotomography of craniosynostosis: review of literature.

Manuela Chiara Accardi1, Elena Lo Magno, Santina Ermito, Angela Dinatale, Alessandra Cacciatore, Alessandro Cavaliere, Diego Rossetti.   

Abstract

Ultrasound examination of the foetal cranium can diagnose fetal cranial defects and abnormal skull shape and it's aim is to detect in prenatal age most various abnormalities of the skull, brain and foetal face. The changes of each of these components frequently determine the growth of the other two.The abnormalities of the foetal head frequently appear and can associate serious pathological sceneries of high foetal and perinatal morbidity and mortality.Anomalies of the head have been observed using ultrasound study during the early second trimester. To establish diagnosis and long term prognosis is particularly important and helpful correct detection of the nature of the malformation.

Entities:  

Keywords:  cranial; fetal; skull; sutures; sypnostosis

Year:  2009        PMID: 22439039      PMCID: PMC3279099     

Source DB:  PubMed          Journal:  J Prenat Med        ISSN: 1971-3282


  16 in total

1.  Clinical spectrum of fibroblast growth factor receptor mutations.

Authors:  M R Passos-Bueno; W R Wilcox; E W Jabs; A L Sertié; L G Alonso; H Kitoh
Journal:  Hum Mutat       Date:  1999       Impact factor: 4.878

Review 2.  Craniosynostosis.

Authors:  Haidar Kabbani; Talkad S Raghuveer
Journal:  Am Fam Physician       Date:  2004-06-15       Impact factor: 3.292

3.  Second-trimester biparietal diameter/nasal bone length ratio is an independent predictor of trisomy 21.

Authors:  Lan T Tran; Darcy B Carr; Lee M Mitsumori; Stefanie B Uhrich; Laurence E Shields
Journal:  J Ultrasound Med       Date:  2005-06       Impact factor: 2.153

4.  Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis.

Authors:  J E Yu; S-Y Jeong; J-A Yang; M S Park; H J Kim; S H Yoon
Journal:  Clin Genet       Date:  2009-07-17       Impact factor: 4.438

5.  Brachycephaly and frontal lobe hypoplasia in fetuses with trisomy 21 at 11 + 0 to 13 + 6 weeks.

Authors:  M Borenstein; T Dagklis; B Csapo; A Sotiriadis; K H Nicolaides
Journal:  Ultrasound Obstet Gynecol       Date:  2006-12       Impact factor: 7.299

6.  Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

Authors:  E W Jabs; X Li; A F Scott; G Meyers; W Chen; M Eccles; J I Mao; L R Charnas; C E Jackson; M Jaye
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

Review 7.  Genetics of craniosynostosis.

Authors:  Virginia Kimonis; June-Anne Gold; Trevor L Hoffman; Jayesh Panchal; Simeon A Boyadjiev
Journal:  Semin Pediatr Neurol       Date:  2007-09       Impact factor: 1.636

8.  Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Authors:  A O Wilkie; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

9.  Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

Authors:  W Reardon; R M Winter; P Rutland; L J Pulleyn; B M Jones; S Malcolm
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

10.  Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.

Authors:  M Oldridge; A O Wilkie; S F Slaney; M D Poole; L J Pulleyn; P Rutland; A D Hockley; M J Wake; J H Goldin; R M Winter
Journal:  Hum Mol Genet       Date:  1995-06       Impact factor: 6.150

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  1 in total

Review 1.  Craniosynostosis - Recognition, clinical characteristics, and treatment.

Authors:  Nina Kajdic; Peter Spazzapan; Tomaz Velnar
Journal:  Bosn J Basic Med Sci       Date:  2018-05-20       Impact factor: 3.363

  1 in total

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