Related Experiment Video
Updated: Mar 29, 2026

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model
Published on: November 4, 2025
A case of familial syndactyly associated with eye and dental abnormalities
Janith K Mills1, Lesley Wheeler, Scott N Oishi
1Janith K. Mills practices at the Charles E. Seay, Jr., Hand Center at Texas Scottish Rite Hospital for Children in Dallas, Tex. Lesley Wheeler is the center's research coordinator. Scott N. Oishi is the center's staff hand surgeon, and is an associate professor in the departments of orthopedic surgery and plastic surgery at the University of Texas Southwestern Medical Center in Dallas. The authors have disclosed no potential conflicts of interest, financial or otherwise.
Abstract:
Syndactyly occurs in 1 in 2,000 live births and is more common in white children. This article describes a patient with syndactyly and additional abnormalities indicating oculodentodigital dysplasia.
Related Concept Videos
Pleiotropy
Nondisjunction
Nondisjunction
Desmosomes
Pedigree Analysis
Genetic Lingo

