Incontinentia pigmenti achromians is a rare birth defect that causes unusual patches of light-colored (hypopigmented) skin and possible neurological and skeletal problems.
See also: Hypopigmentation
Hypomelanosis of Ito (more commonly used)
The cause is unknown. It is slightly more common in girls than in boys.
Crossed eyes (strabismus)
- Increased body hair (hirsutism)
- Streaked, whirled or mottled patchs of skin on the arms, legs, and middle of the body
- Varying degrees of retardation
A Wood's lamp examination of the skin lesions may help confirm the diagnosis. Your doctor may also recommend chromosome analysis or a further medical workup to discover any related medical problems.
What happens depends on the type and severity of symptoms that develop. In most cases, the skin pigment eventually returns to normal.
Call your health care provider if your child exhibits an unusual pattern of the color of the skin.
- Discomfort and walking problems due to scoliosis
- Emotional distress related to the physical appearance
- Seizures and resulting possible injury
There is no treatment for the hypopigmentation. Treatment consists of treating the symptoms. Cosmetics or clothing may be used to cover the hypopigmented spots if desired. Seizures, scoliosis, and other problems are treated as necessary.
Genodermatoses and Congenital Anomolies. In: James WD, Berger TG, Elston DM, eds. Andrews' Diseases of the Skin: Clinical Dermatology. 10th ed. Philadelphia, Pa: Saunders Elsevier; 2005: chap 27.
Moss C. Mosaicism and Linear Lesions. In: Bolognia JL, Jorizzo JL, Rapini RP, eds.: Dermatology. 2nd ed. Philadelphia, Pa: Mosby Elsevier; 2008: chap 61.
Review Date: 8/26/2009
Reviewed By: Kevin Berman, MD, PhD, Atlanta Center for Dermatologic Disease, Atlanta, GA. Review provided by VeriMed Healthcare Network; Linda Vorvick, MD, Medical Director, MEDEX Northwest Division of Physician Assistant Studies, University of Washington School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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