Nuchal thickening in Jacobsen syndrome

Ultrasound in Obstetrics and Gynecology

Volumn 12, Issue 4, 1998, Pages 280-282

  McClelland, S M ^a,b   Smith, A P M ^b   Smith, N C ^b   Gray, E S ^a   Diack, J S W ^a   Dean, J C S ^a  

^a Department of Radiology ^*  (United Kingdom)

^b ABERDEEN ROYAL INFIRMARY   (United Kingdom)

Author keywords

Amniocentesis; Chromosome 11q deletion; Jacobsen syndrome; Nuchal thickening

Indexed keywords

ALPHA FETOPROTEIN;

ADULT; AMNIOCENTESIS; ARTICLE; AUTOPSY; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME ANALYSIS; CLINICAL FEATURE; FEMALE; FETUS ECHOGRAPHY; FETUS MALFORMATION; GESTATIONAL AGE; HUMAN; KARYOTYPE 46,XY; PHENOTYPE; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0031796007     PISSN: 09607692     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-0705.1998.12040280.x     Document Type: Article

References (13)

1. Jacobsen P, Hauge M, Henningsen K, Hobolth N, Middleson M, Philip J. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. Hum Hered 1973;23:568-85
2. Lewanda AF, Morsey S, Reid CS, Jabs EW. Two craniostenotic patients with 11q deletions, and review of 48 cases. Am J Med Genet 1995;59:193-8
3. Fryns JP, Kleczowska A, Buttiens M, Marien P, Van den Berge H. Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1. Clin Genet 1986;30:255-60
4. O'Hare AE, Grace E, Edmunds AT. Deletion of the long arm of chromosome 11[46,XX,del(11) (q24.1 →qter)]. Clin Genet 1984;13:373-7
5. Voullaire LE, Webb GC, Leversha MA. Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23. Hum Genet 1987;76:202-4
6. Wax JR, Smith JF, Floyd RC, Eggleston MK. Prenatal ultrasonographic findings associated with Jacobsen syndrome. Ultrasound Med 1995;14:256-8
7. Dawson AJ, Marles SL, Harman CR, Menticolou S. Prenatal diagnosis of ring chromosome 6. Prenat Diagn 1995;15: 872-4
8. Jean M, Rival JM, Mensier S, Lopes P. Prenatal diagnosis of ring chromosome 14 after intracytoplasmic sperm injection. Fertil Steril 1997;67:164-5
9. Hyett JA, Clayton PT, Moscoso G, Nicolaides KH. Increased nuchal translucency as a prenatal manifestation of Smith-Lemli-Opitz syndrome. Am J Med Genet 1995;58: 374-6
10. Hyett JA, Perdu M, Sharland GK, Snijders RSM, Nicolaides KH. Increased nuchal translucency at 10-14 weeks of gestation as a marker for major cardiac defects. Ultrasound Obstet Gynecol 1997;10:242-6
11. Nicolaides KH, Azar G, Snijders RSM, Gosden CM. Fetal nuchal oedema: associated malformations and chromosomal defects. Fetal Diagn Ther 1992;7:123-31
12. Sirota L, Shabtai F, Landma I, Halbrecht I, Dulitzky F. New anomalies found in the 11q-syndrome. Clin Genet 1984;26: 569-73
13. Kaffe S, Hsu LYF, Sachdev RK, Philips J, Hirschhorn K. Partial deletion of long arm of chromosome 11:del(11)(q23). Clin Genet 1977;12:323-8