Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2012 Jan;27(1):54-5.
doi: 10.5001/omj.2012.11.

Fetal amelia: a case report

Case Reports

Fetal amelia: a case report

Nihal Al Riyami et al. Oman Med J. 2012 Jan.

Abstract

Congenital limb defects are rare fetal anomalies with a birth prevalence of 0.55 per 1,000. Amelia is an extremely rare birth defect marked by the complete absence of one or more limbs. We report a case of fetal amelia, ultrasound findings, manifestations and the fetal outcome.

Keywords: Amelia; Congenital; Limb defects; Rare; Sporadic.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The baby gram.
Figure 2
Figure 2
External examination of the stillborn baby.
Figure 3
Figure 3
Examination of the genital area of the stillborn baby.

References

    1. Lenz W. Genetics and limb deficiencies. Clin Orthop Relat Res 1980. May;(148):9-17 - PubMed
    1. Froster-Iskenius UG, Baird PA. Amelia: incidence and associated defects in a large population. Teratology 1990. Jan;41(1):23-31 10.1002/tera.1420410104 - DOI - PubMed
    1. Evans JA, Vitez M, Czeizel A. Patterns of acrorenal malformation associations. Am J Med Genet 1992. Nov;44(4):413-419 10.1002/ajmg.1320440405 - DOI - PubMed
    1. Mastroiacovo P, Källén B, Knudsen LB, Lancaster PA, Castilla EE, Mutchinick O, et al. Absence of limbs and gross body wall defects: an epidemiological study of related rare malformation conditions. Teratology 1992. Nov;46(5):455-464 10.1002/tera.1420460510 - DOI - PubMed
    1. Smithells RW, Newman CG. Recognition of thalidomide defects. J Med Genet 1992. Oct;29(10):716-723 10.1136/jmg.29.10.716 - DOI - PMC - PubMed

Publication types

LinkOut - more resources