Article

Cantú Syndrome and Endocrine Monitoring: A Pediatric Case Report

2026-08-28

Abstract excerpt

<h4>Introduction: </h4> Cantú syndrome, or hypertrichotic osteochondrodysplasia, is a rare genetic disorder characterized by generalized hypertrichosis, macrosomia, cardiomegaly, and distinctive coarse facial features. What is unique about this case is the clinical challenge of distinguishing syndromic hypertrichosis from premature pubarche in early childhood, emphasizing the necessity for multidisciplinary and ta...

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Literature Corpus work: daf29c97-667c-52a4-b88d-6dc5a066533a
DOI: 10.20944/preprints202608.2048.v1

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