Acrorenal ocular syndrome: Case series of a rare familial congenital syndrome

Autor: Rajagopal Ganesh, S. Shanmuga Jayanthan, N. Karunakaran, G. Rupesh, K. Nadanasadharam, Sidramappa Dande
Rok vydání: 2023
Zdroj: Case Reports in Clinical Radiology. :1-4
ISSN: 2836-0788
DOI: 10.25259/crcr_50_2022
Popis: Acrorenal ocular syndrome includes a spectrum of acral anomalies such as oligodactyly, ectrodactyly, syndactyly, brachydactyly, humerus/carpal hypoplasia, cutaneous syndactyly, and renal anomalies such as unilateral renal agenesis, unilateral hypoplasia, ectopia, horseshoe kidney, and vesico-ureteric reflex. The common ocular manifestations include Duane anomaly, coloboma, and ptosis.
Databáze: OpenAIRE