Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism

Figure 2

A pedigree showing inherited mutations. Filled symbol indicates the affected individual. Chromatograms of the point mutations identified in the affected individual are shown (a). HE, original magnification x200: skin biopsy showing hyperkeratosis, acanthosis, and absence of the granular layer (b). Light microscopy typical of trichorrhexis invaginata (bamboo hair) (c).

(a)

(b)

(c)