References 1 Berron-Ruiz A, Berron-Perez R, Ruiz-Maldonado R. Cutaneous markers of primary immunodeficiency diseases in children. Pediatr Dermatol 2000; 17: 91-96. 2 Van Dongen JJ, Langerak AW, Bruggemann M et al. Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936. Leukemia 2003; 17: 2257-2317. 3 Bentur L, Shear N, Roifman CM. Cutaneous lymphohistiocytic infiltrates in patients with hypogammaglobulinemia. J Pediatr 1990; 116: 68-72. 4 Fleming MG, Gewurz AT, Pearson RW. Caseating cutaneous granulomas in a patient with X-linked infantile hypogammaglobulinemia. J Am Acad Dermatol 1991; 24: 629-633. 5 Park JY, Kim YS, Shin DH et al. Primary cutaneous peripheral T-cell lymphoma in a patient with X-linked agammaglobulinaemia. Br J Dermatol 2011; 164: 677-679. 6 Petrella T, Maubec E, Cornillet-Lefebvre P et al. Indolent CD8-positive lymphoid proliferation of the ear: a distinct primary cutaneous T-cell lymphoma? Am JEADV 2016, 30, 446-556 464 Letters to the EditorThis report provides additional evidence that LMNA mutations are associated with HGPS and a broad spectrum of associated clinical features. This finding will contribute to the understanding of the pathogenesis of HGPS and allow relevant clinical phenotypic traits to be predicted and treated.
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