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A Rare Bond: Exploring the Heart-Hand Connection in Holt-Oram Syndrome

Year: 2024
Type: article
Study design: Case Report
Abstract: Holt-Oram syndrome is an autosomal dominant disorder characterized by upper limb abnormalities in association with congenital heart lesions. We present you a 42 years old female having ostium secundum atrial septal defect (OS-ASD) and congenital upper limb deformity. Her X-ray of hands showed bilateral abnormal carpal bones with underdeveloped thumb. This study highlights the importance of recognizing the heart-hand connection in Holt-Oram syndrome and presents the need for multidisciplinary care and early intervention.
Language: English
Open Access status: diamond
OpenAlex ID: W4405551736
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