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The disease is caused by a mutation of the ikbkg gene It is characterised by distinct and changing skin lesions with or without associated teeth, hair,. This rare disorder presents in the first few weeks of.

Incontinentia pigmenti (ip) is a genetic disorder with distinctive skin rashes and lesions seen at birth or within the first few weeks This condition occurs much more often in females than in males The majority of children with ip don’t have complications and.

It is named from its appearance under a microscope.

Incontinentia pigmenti is a rare genetic condition characterised by skin, eye, teeth and central nervous system (cns) abnormalities The characteristic skin lesions of incontinentia pigmenti. Incontinentia pigmenti (ip) is a genetic ectodermal dysplasia affecting the skin, hair, teeth, microvasculature and central nervous system Progressive skin changes occur in.

Incontinentia pigmenti is a condition that can affect many body systems, particularly the skin

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