Unilateral Transverse Arm Defect with Subterminal Digital Nubbins

Author:

Drapkin Ronny I.12,Genest David R.12,Holmes Lewis B.3,Huang Taosheng4,Vargas Sara O.125

Affiliation:

1. Department of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA

2. Department of Pathology, Harvard Medical School, Boston, MA, USA

3. Genetics and Teratology Unit, Pediatric Service, Massachusetts General Hospital, Boston, MA, USA

4. Division of Genetics and Metabolism, Children's Hospital, Boston, MA, USA

5. Department of Pathology, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA

Abstract

We present a case of unilateral terminal transverse forearm deficiency with subterminal digit-like nubbins, identified in a fetus from a pregnancy terminated electively in the second trimester because the distal right arm and hand could not be seen by ultrasound and were presumed to be absent. Pathologic evaluation showed distal transverse shortening, tapering to a point in the mid-forearm. Five primitive digital nubbins were present, located just proximal to the tapered point. The arm vessels appeared normal histologically, and the amnion showed no evidence of intrauterine disruption. Histologic examination of the nubbins revealed osteocartilaginous tissue, never described previously within digital nubbins. This fetus has the rare phenotype of terminal transverse limb defects with residual nubbins, but differs in that the nubbins are not at the tip of the terminal transverse limb defect.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

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1. Terminal transverse limb defects;Birth Defects Research;2021-07-14

2. Terminal transverse limb defects with “nubbins”;Birth Defects Research;2021-07-08

3. Malformations attributed to the process of vascular disruption;Birth Defects Research;2018-01

4. Causes of Congenital Malformations;Birth Defects Research;2018-01

5. Anatomic and etiological classification of congenital limb deficiencies;American Journal of Medical Genetics Part A;2011-05-09

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