Incontinentia Pigmenti

National Organization for Rare Disorders, Inc.

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  • pigmented dermatosis, Siemens-Bloch type
  • IP
  • Bloch-Sulzberger syndrome
  • Bloch-Siemens incontinentia pigmenti melanoblastosis cutis linearis

Disorder Subdivisions

  • None

General Discussion


Incontinentia Pigmenti (IP) is a rare genetic dermatological disorder affecting the skin, hair, teeth, and central nervous system. Progressive skin changes occur in four stages, the first of which appear in early infancy or can be present at birth. IP is an X-linked dominant genetic disorder caused by mutations in the IKBKG gene.


IP was named based on the appearance of the skin under the microscope.


The first stage of IP may be present at birth or appear during early infancy. This phase consists of redness or inflammation of the skin (erythema), blisters, and boils, most often affecting the extremities and the scalp, that last a few weeks to a few months. It can fade and come back again and again for more than a year, commonly when there is a illness with fever. The second stage may overlap the first and may be present at birth. During this phase, the blisters develop a raised, wart-like (verrous) appearance, and the lesions look like pustules. There can be thick crusts or scabs with healing and areas of darkened skin (increased pigmentation). The extremities are involved almost exclusively in this stage, which may last for several months but rarely as long as year. The third stage may be present at birth in a small number of affected individuals, but usually appears between the ages of six and 12 months. In this phase, the skin is darkened (hyperpigmented). On the trunk, the dark areas appear in a swirled pattern sometimes described as a "marble cake" appearance. On the extremities it is linear. Dark areas can appear on the face: the hyperpigmentation does not necessarily happen where the stage I and II rashes happen. The heavy pigmentation tends to fade over time and, in some cases, the pigmented areas thin and widen, leaving streaky diminished color of the skin (hypopigmentation). In the fourth stage, which is known as the "atrophic" stage, scarring appears that often is present before the hyperpigmentation has faded. Scars are seen in adolescents and adults as pale, hairless patches or streaks. Once the affected individuals reach the late teens and adulthood, the skin changes may have faded and may not be visible to the casual observer.

Between 50 to 75 percent of individuals with IP have dental abnormalities. These abnormalities include a delay in the eruption of primary teeth; abnormal contours of teeth, giving them a peg-like or cone-shaped appearance; or the congenital absence of both primary and secondary teeth (anodontia); or small teeth, (microdontia).

Some individuals with IP may have ridged, pitted, thickened (onychogryposis), or missing nails on the hands and/or feet. In some cases, painful growths may develop under the nail.

Approximately 50 percent of individuals with IP may also experience abnormal bald patches on the scalp (alopecia). The hair generally may be coarse, wiry, and/or lusterless.

Nearly one-third of individuals have eye (ocular) abnormalities. This can include a congenitally small, abnormal eye. An abnormality in the growth of blood vessels in the membrane lining the eyes (retina), which typically appears before the age of five, may be treated if detected early but may cause retinal detachment leading to permanent visual impairment or total blindness if left untreated.

Although the majority of individuals with IP will have no involvement of the nervous system, severe neurologic complications can occasionally occur as a consequence of IP. Some affected individuals may experience episodes of uncontrolled electrical disturbances in the brain (seizures). About 20 percent of children with IP will have slow motor development, muscle weakness in one or both sides of the body, intellectual disability, and seizures.

Abnormalities in the development of the breast, ranging from extra nipples to complete absence of the breast, are sometimes seen in individuals with IP.


IP is an X-linked dominant genetic disorder caused by mutations in the IKBKG gene. The IKBKG gene is responsible for the production of a protein that helps regulate other proteins called nuclear factor-kappa-B that help protect cells from self-destructing in response to specific triggers.

X-linked dominant disorders are caused by an abnormal gene on the X chromosome and occur mostly in females. Females with these rare conditions are affected when they have an X chromosome with the gene for a particular disease. Males with an abnormal gene for an X-linked dominant disorder are more severely affected than females and often do not survive. Affected males who survive may have an IKBKG gene mutation with relatively mild effects, an IKBKG mutation in only some of the body's cells (mosaicism), or an extra copy of the X chromosome in each cell.

Affected Populations

Approximately 900 to 1,200 individuals with IP have been reported in the scientific literature. Most of those affected are female, but several dozen males with IP have also been reported.

Standard Therapies


The diagnosis of IP is based on clinical evaluation, detailed patient history, and molecular genetic testing for mutation in the IKBKG (previously called NEMO) gene. IKBKG is the only gene known to be associated with IP. Mutations in this gene are present in about 80% of affected individuals. A skin biopsy to confirm the diagnosis in a female is now rarely needed given the widespread availability and sensitivity of molecular genetic testing. Nonetheless, skin biopsy may be helpful in confirming the diagnosis in a female with borderline or questionable findings in whom molecular genetic testing has not identified a disease-causing mutation.

Clinical Testing and Work-Up

It is very important for babies born with IP to have an eye examination by an ophthalmologist. This should be done monthly until age four months, then every three months from age four months to one year, every six months from age one to three years, and annually after age three years. The eye problems associated with IP can be severe, but may be effectively managed if recognized early.

The following evaluations may be done to determine the severity of disease in those affected with IP: physical examination with particular emphasis on the skin, hair, nails, and neurologic system, electroencephalography (EEG) and magnetic resonance imaging (MRI) if seizures, other neurologic abnormalities, or retinal abnormalities are present, magnetic resonance angiography to look for cerebrovascular lesions, and developmental screening.

Because IP can be very mild, even in infancy, an affected woman may not know that she has it. It is important that a full evaluation of the mother be done by a geneticist, dermatologist, or other physician after the birth of a child with IP.


Skin abnormalities characteristic of IP (IP) usually disappear by adolescence or adulthood without any treatment.

Cryotherapy and laser photocoagulation may be used to treat affected individuals with retinal neovascularization that predisposes to retinal detachment.

Dental abnormalities can often be treated effectively by dentists who may provide dental implants in childhood as needed. Also if dental abnormalities interfere with chewing and/or speech, assistance from a speech pathologist and/or pediatric nutritionist may be necessary

Hair problems may require the attention of a dermatologist in some cases, although they are usually not severe. Neurological symptoms such as seizures, muscle spasms or mild paralysis may be controlled with various drugs and/or medical devices.

Genetic counseling is recommended for affected individuals and their families. Other treatment is symptomatic and supportive.

Investigational Therapies

Information on current clinical trials is posted on the Internet at All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.

For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:

Tollfree: (800) 411-1222

TTY: (866) 411-1010


For information about clinical trials sponsored by private sources, contact:

For information about clinical trials conducted in Europe, contact:

Contact for additional information about incontinentia Pigmenti:

Angela Scheuerle, M.D.

Tesserae Genetics

7777 Forest Lane, B240

Dallas TX 75230

Phone: 972 566 6524

Fax: 972 566 2024



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Nelson DL. NEMO, NFkappaB signaling and incontinentia pigmenti. Curr Opin Genet Dev. 2006;16(3):282-8.

Käsmann-Kellner B, Jurin-Bunte B, Ruprecht KW. Incontinentia pigmenti (Bloch-Sulzberger-syndrome): case report and differential diagnosisto related dermato-ocular syndromes. Ophthalmologica. 1999;213(1):63-9.

Goldberg MF. Macular vasculopathy and its evolution in incontinentia pigmenti. Ophthalmic Genet. 1998;19(3):141-8.

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Scheuerle A, Ursini MV. (Updated October 28, 2010). Incontinentia Pigmenti. In: GeneReviews at GeneTests: Medical Genetics Information Resource (database online). Copyright, University of Washington, Seattle. 1997-2012. Available at Accessed November 16, 2012.

Online Mendelian Inheritance in Man (OMIM). The Johns Hopkins University. Incontinentia Pigmenti; IP. Entry No: 308300. Last Edited December 16, 2011. Available at: Accessed November 16, 2012.

Incontinentia Pigmenti. Genetics Home Reference. Reviewed June 2008. Accessed November 16, 2012.


National Foundation for Ectodermal Dysplasias

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March of Dimes Birth Defects Foundation

1275 Mamaroneck Avenue

White Plains, NY 10605

Tel: (914)997-4488

Fax: (914)997-4763


Incontinentia Pigmenti International Foundation

30 East 72nd Street

Suite 16

New York, NY 10021


Tel: (212)452-1231

Fax: (212)452-1406



NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases

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Genetic and Rare Diseases (GARD) Information Center

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Madisons Foundation

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Tel: (310)264-0826

Fax: (310)264-4766



Ectodermal Dysplasia Society

Unit 1 Maida Vale Business Centre




England, GL53 7ER

United Kingdom

Tel: 4401242261332

Tel: 4407805775703



For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see