Hypochondroplasia Foundation
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    • Home
    • About Us
      • About Us
      • Mission
      • Medical Advisory Board
      • Advisory Council
      • Board of Directors
      • Webinars
      • Helpline
      • Partners
      • Get Involved
    • For Families
      • Practical Guides
      • Facebook Group
      • Latest News
      • Possible Diagnosis
      • New Diagnosis
      • Understanding HCH
      • Neurological Symptoms
      • Childhood
      • Teenage Years
      • Adulthood
      • Ear, Nose and Throat
      • Treatment Options
      • Family Support
      • HCH FAQ
    • Research
      • Research Overview
      • Clinical Trials
      • Patient Registry
      • Publications
      • Research Participation
      • For Medical Professionals
      • Research Partners
      • Genetic Testing
      • FGFR3 and the Brain
      • Ear, Nose and Throat
      • Library
    • Contact Us
Hypochondroplasia Foundation
  • Home
  • About Us
    • About Us
    • Mission
    • Medical Advisory Board
    • Advisory Council
    • Board of Directors
    • Webinars
    • Helpline
    • Partners
    • Get Involved
  • For Families
    • Practical Guides
    • Facebook Group
    • Latest News
    • Possible Diagnosis
    • New Diagnosis
    • Understanding HCH
    • Neurological Symptoms
    • Childhood
    • Teenage Years
    • Adulthood
    • Ear, Nose and Throat
    • Treatment Options
    • Family Support
    • HCH FAQ
  • Research
    • Research Overview
    • Clinical Trials
    • Patient Registry
    • Publications
    • Research Participation
    • For Medical Professionals
    • Research Partners
    • Genetic Testing
    • FGFR3 and the Brain
    • Ear, Nose and Throat
    • Library
  • Contact Us

Webinars

Diagnosing Hypochondroplasia - International Recommendations  - Andrew Dauber MD  - Oct 2026

 

Hypochondroplasia can be difficult to recognise, particularly in young children and people with more subtle features. For many families, reaching a clear diagnosis can involve years of uncertainty.


In this episode, we welcome Dr Andrew Dauber, co-lead author of the international diagnostic recommendations published in August 2026, to discuss why this guidance was needed and what it means for families.

ENT Concerns in Hypochondroplasia | Dr Alessandra Cocca - Oct 2026


Ear, nose and throat (ENT) concerns in hypochondroplasia have received relatively little attention, and many families may not be aware of the symptoms to look out for or when to seek specialist advice.



In this episode, we welcome Dr Alessandra Cocca, Consultant in Paediatric Endocrinology and Bone and Mineral Disorders at Evelina London Children's Hospital, to discuss findings from a retrospective study of 49 patients with HCH.


Copyright © 2026 Hypochondroplasia Foundation.  Register Number: 819128 - Ireland - All Rights Reserved.

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