Sindrome de Leri-Weill - Discondrosteose

🎯 Schedule Your Consultation With the Specialist Now (Online or In-Person)! https://bit.ly/drcaiobruzaca Leri-Weill syndrome is a rare genetic disease that primarily affects bone growth and stature. In this video, I explain what Leri-Weill syndrome, also called dyschondrosteosis, is and what its main characteristics are. You will understand that this condition is usually related to genetic alterations that interfere with the normal development of bones, especially in the arms and legs. This can lead to disproportionate short stature and changes in limb shape. Throughout the video, I explain the main signs of Leri-Weill syndrome, such as shortening of the mid-segments of the limbs, bone alterations, and deformities that may arise during growth. I also show how the diagnosis is made through clinical evaluation, imaging exams, and genetic investigation, allowing for a more precise identification of the cause of the condition. Another important point is understanding that, despite being a rare disease, early recognition helps with proper monitoring and individualized therapeutic planning. In the end, you will understand what Leri-Weill syndrome is, how it manifests, and why a correct diagnosis makes such a difference. ⏱️ Video Chapters: 00:00 – What is Leri-Weill syndrome? 01:20 – Why does dyschondrosteosis occur? 02:50 – Main signs and symptoms 04:20 – Changes in bone growth 05:50 – How is the diagnosis made? 07:10 – Monitoring and care 08:20 – Final conclusions 🧩 In this video: Understand what Leri-Weill syndrome is Discover the signs of dyschondrosteosis Learn how the diagnosis is made See the importance of early monitoring 🎯 Schedule Your Consultation With the Specialist Now (Online or In-Person)! Leri-Weill Syndrome - Dyschondrosteosis https://bit.ly/drcaiobruzaca    • Sindrome de Leri-Weill - Discondrosteose