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Familial CaLS may correspond to a form of Legius syndrome, although this has been ruled out in some cases.24 Mosaic forms of NF1 may exist exclusively with cutaneous involvement and NF1 mutations may not be detectable in circulating leukocytes.19 It may even be the case that the mutation resides in another gene of the RAS pathway.33,34 McCune-Albright syndrome is characterized by extensive CaLS, often with a unilateral segmental distribution and irregular borders

coli result points to fecal contamination, which is the more serious finding

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It is a synthetic peptide fragment consisting of 16 amino acids taken from the C-terminal end of human growth hormone, specifically residues 177 through 191