Peters anomaly in cri-du-chat syndrome
William C Hope1, Jose A Cordovez2, Jenina E Capasso2
1Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania.
Abstract:
The cri-du-chat syndrome is a rare genetic disorder caused by deletions in the short arm of chromosome 5. It presents with a distinctive catlike high-pitched cry, psychomotor delays, microcephaly, craniofacial abnormalities, and, in many cases, ocular findings. We report the first child with cri-du-chat and the findings of unilateral corneal staphyloma due to Peters anomaly and retinal dysplasia.
More Related Videos
12:47Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
10:23Author Spotlight: Three-Dimensional Cephalometric Landmark Annotation Demonstration on Human Cone Beam Computed Tomography Scans
Published on: September 8, 2023
Related Concept Videos
Karyotyping
Pedigree Analysis
Incomplete Dominance
Microtubules in Signaling
Meiosis I
Nondisjunction
