Apert syndrome associated with increased fetal nuchal translucency [6]

Prenatal Diagnosis

Volumn 25, Issue 11, 2005, Pages 1066-1067

  Aleem, S ^a   Howarth, E S ^a  

^a LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; CARDIOTOCOGRAPHY; CASE REPORT; CESAREAN SECTION; CHORION VILLUS SAMPLING; CRANIOFACIAL SYNOSTOSIS; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DOWN SYNDROME; FETOSCOPY; FETUS; FETUS ECHOGRAPHY; FETUS KARYOTYPING; HUMAN; LETTER; MECONIUM ASPIRATION; PRENATAL DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL;

ACROCEPHALOSYNDACTYLIA; FATAL OUTCOME; FEMALE; FETAL DISEASES; HUMANS; INFANT, NEWBORN; MALE; NUCHAL TRANSLUCENCY MEASUREMENT; PREGNANCY; PRENATAL DIAGNOSIS; RECEPTORS, FIBROBLAST GROWTH FACTOR;

EID: 28544442308     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1294     Document Type: Letter

References (11)

1. Allanson JE. 1986. Germinal mosaicism in Apert Syndrome. Clin Genet 29: 429-433.
2. Chenoweth-Mitchell C, Cohen GR. 1994. Prenatal sonographic findings of Apert Syndrome. J Clin Ultrasound 22(8): 510-514.
3. Cohen MM Jr, Kreiborg S, Lammer EJ, et al. 1992. Birth prevalence study of the Apert Syndrome. Am J Med Genet 42: 655-659.
4. Ferreira JC, Carter SM, Bernstein PS, et al. 1999. Second-trimester molecular prenatal diagnosis of sporadic Apert Syndrome following suspicious ultrasound findings. Ultrasound Obstet Gynecol 14: 426-430.
5. Filkins K, Russo JF, Boehmer S, et al. 1997. Prenatal ultrasonographic and molecular diagnosis of Apert Syndrome. Prenat Diagn 17(11): 1081-1084.
6. Kaplan L. 1991. Clinical assessment and multispecialty management of Apert Syndrome. Clin Plast Surg 18(2): 217-225.
7. Kim H, Uppal V, Wallach R. 1986. Apert Syndrome and fetal hydrocephaly. Hum Genet 73: 93-95.
8. Leonard CO, Daikoku NH, Winn K. 1982. Prenatal fetoscopic diagnosis of the Apert Syndrome. Am J Med Genet 11: 5-9.
9. Patton MA, Goodship J, Hayward R, Lansdown R. 1988. Intellectual development in Apert's Syndrome: a long term follow up of 29 patients. J Med Genet 25: 164-167.
10. Tolarova MM, Harris JA, Ordway DE, Vargervik K. 1997. Birth prevalence, mutation rate, sex ratio, parents' age and ethnicity in Apert Syndrome. Am J Med Genet 72: 394-398.
11. Wilkie AOM, Slaney SF, Oldridge M, et al. 1995. Apert Syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 9: 165-172.