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Incontinentia pigmenti syndrome
- ... Bloch-Sulzberger Syndrome IP Genetic Testing Registry: Incontinentia pigmenti syndrome Incontinentia pigmenti National Organization for Rare Disorders (NORD) ClinicalTrials. ...
- Incontinentia Pigmenti (National Institute of Neurological Disorders and Stroke)Incontinentia pigmenti (IP) is an inherited (genetic) condition that affects the skin and other systems in the body. ...
- Incontinentia pigmenti (IP) is a rare skin condition passed down through families. It affects the skin, hair, eyes, ... Organization for Rare Disorders -- rarediseases.org/rare-diseases/incontinentia-pigmenti/
- Incontinentia pigmenti causes swirling pigmentation of the skin. It is seen more frequently in females. The skin lesions ...
- Incontinentia pigmenti produces darkly-pigmented swirling marks on the skin. It occurs more frequently in females. The skin ...
- Incontinentia pigmenti produces darkly-pigmented swirling marks on the skin. It occurs more frequently in females. The skin ...
- Hypomelanosis of Ito (HMI) is a very rare birth defect that causes unusual patches of light-colored ( hypopigmented ) skin and may be associated ...
- Ectodermal dysplasias is a group of conditions in which there is abnormal development of the skin, hair, nails, teeth, or sweat glands.
- ... IKBKG gene have been identified in people with incontinentia pigmenti, a condition characterized by skin, tooth, and nail ... The most common IKBKG gene variant that causes incontinentia pigmenti is a complex rearrangement that deletes some genetic ...
- Skin Pigmentation Disorders (National Library of Medicine)Pigmentation means coloring. Skin pigmentation disorders affect the color of your skin. Your skin gets its color from a pigment called melanin. Special cells in the ...