Syndromes associated with hyperpigmented macules

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Incontinentia pigmenti. Deletion of exons 4-10 of the IKBKG gene [1 gene]

Ref.: S-202212864

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Incontinentia pigmenti. Sequencing of the IKBKG gene by Sanger [1 gene]

Ref.: S-202009380

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Lentiginosis [10 genes]

Ref.: S-202313134

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McCune-Albright syndrome. GNAS gene sequencing. NextGeneDx [1 gene]

Ref.: S-202314051

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Syndromes associated with café-au-lait spots [60 genes]

Ref.: S-202313135