A brief overview

WHS at a glance

A Brief Overview

WHS at a glance

Wolf-Hirschhorn syndrome (WHS) is a rare genetic condition caused by a deletion on the short arm of chromosome 4. Because of this, it is sometimes also known as 4p-minus syndrome.

WHS is estimated to affect around 1 in 50,000 births, although exact numbers are difficult to determine.

Wolf-Hirschhorn syndrome (WHS) affects many parts of the body. It is characterized by a distinct set of physical features and developmental delays. Every child and adult with WHS is unique. The condition can affect development, growth, health and learning in different ways.

Symptoms vary widely, and no two individuals will experience the condition in exactly the same way.

Some common signs include:

Make a Difference

Make a Difference

Your support helps us provide vital information, practical assistance, and a strong sense of community for individuals and families affected by Wolf-Hirschhorn Syndrome. Every donation, no matter the size, helps us continue our work and reach those who need us most.

Follow Us

Follow Us

We share snapshots of life within the Wolf-Hirschhorn Syndrome community, from awareness and events to family experiences and milestones. It’s a place to stay connected and see the impact of our work in real time.