Hypomelanosis of Ito (HMI) is a very rare birth defect that causes unusual patches of light-colored (hypopigmented) skin and may be associated with eye, nervous system, and skeletal problems.
Health care providers do not know the exact cause of HMI, but they believe it is a problem with genes. It is twice as common in girls than in boys.
Skin symptoms are most often visible by the time a child is about 2 years old.
Other symptoms develop as the child grows, and may include:
Exams and Tests
Ultraviolet light (Wood lamp) examination of the skin lesions may help confirm the diagnosis.
Tests that may be done include any of the following:
There is no treatment for the skin patches. Cosmetics or clothing may be used to cover the patches. Seizures, scoliosis, and other problems are treated as needed.
Outlook depends on the type and severity of symptoms that develop. In most cases, skin color eventually turns to normal.
Problems that may result from HMI include:
- Discomfort and walking problems due to scoliosis
- Emotional distress, related to the physical appearance
- Intellectual disability
- Injury from seizures
When to Contact a Medical Professional
Call your provider if your child has an unusual pattern of the color of the skin. However, any unusual patterns are likely to have another cause than HMI.
Incontinentia pigmenti achromians; HMI; Ito hypomelanosis
Habif TP. Light-related diseases and disorders of pigmentation. In: Habif TP, ed. Clinical Dermatology: A Color Guide to Diagnosis and Therapy. 6th ed. Philadelphia, PA: Elsevier; 2016:chap 19.
Patterson JW. Disorders of pigmentation. In: Patterson JW, ed. Weedon's Skin Pathology. 4th ed. Philadelphia, PA: Elsevier Churchill Livingstone; 2016:chap 10.
Review Date 5/2/2017
Updated by: David L. Swanson, MD, Vice Chair of Medical Dermatology, Associate Professor of Dermatology, Mayo Medical School, Scottsdale, AZ. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.