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Reticulate hyperpigmentation.
Schnur RE, Heymann WR. Schnur RE, et al. Semin Cutan Med Surg. 1997 Mar;16(1):72-80. doi: 10.1016/s1085-5629(97)80038-7. Semin Cutan Med Surg. 1997. PMID: 9125768 Review.
The most common pattern of inheritance is X-linked, with heterozygous females showing variable expression, most likely depending on tissue-specific patterns of random X-inactivation. Other reticulate pigmentary disorders reviewed include the Naegeli-Franceschetti-Jadassohn …
The most common pattern of inheritance is X-linked, with heterozygous females showing variable expression, most likely depending on tissue-s …
Dermatopathia Pigmentosa Reticularis with Salzmann's nodular degeneration of cornea: A rare association.
Goel R, Bodh SA, Sardana K, Goel A. Goel R, et al. Nepal J Ophthalmol. 2015 Jan-Jun;7(1):79-81. doi: 10.3126/nepjoph.v7i1.13175. Nepal J Ophthalmol. 2015. PMID: 26695611
BACKGROUND: Dermatopathia pigmentosa reticularis (DPR) is a very rare autosomal dominant disorder with the diagnostic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia and onychodystrophy. OBJECTIVE: To describe the occurrence of Salz …
BACKGROUND: Dermatopathia pigmentosa reticularis (DPR) is a very rare autosomal dominant disorder with the diagnostic t …