Isolated fetal macrodactyly: phenotypic and genetic disparities in mosaic overgrowth syndrome

J Ultrasound Med. 2014 Jul;33(7):1305-7. doi: 10.7863/ultra.33.7.1305.

Authors

Eran Bornstein¹, Carlos A Bacino¹, Kristen Maliszewski¹, Kim Delaney¹, Reut Moyal¹, Michael Y Divon¹

Affiliation

¹ Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Lenox Hill Hospital, New York, New York USA (E.B., K.D., R.M., M.Y.D.); Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas USA (C.A.B., K.M.).

PMID: 24958419
DOI: 10.7863/ultra.33.7.1305

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Class I Phosphatidylinositol 3-Kinases
Female
Fetal Diseases / genetics*
Fingers / abnormalities*
Fingers / diagnostic imaging
Humans
Limb Deformities, Congenital / diagnostic imaging*
Limb Deformities, Congenital / genetics*
Phenotype
Phosphatidylinositol 3-Kinases / genetics
Syndrome
Translocation, Genetic
Ultrasonography, Prenatal

Substances

Phosphatidylinositol 3-Kinases
Class I Phosphatidylinositol 3-Kinases
PIK3CA protein, human

Supplementary concepts

Megalodactyly