• Thumbnail for Dermatopathia pigmentosa reticularis
    Dermatopathia pigmentosa reticularis (DPR) is a rare, autosomal dominant congenital disorder that is a form of ectodermal dysplasia. Dermatopathia pigmentosa...
    13 KB (1,309 words) - 09:19, 10 August 2024
  • Thumbnail for Albinism in humans
    Reticulated Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly...
    39 KB (3,840 words) - 06:15, 20 August 2024
  • Thumbnail for List of skin conditions
    syndrome) Dermatopathia pigmentosa reticularis (dermatopathia pigmentosa reticularis hyperkeratotica et mutilans, dermatopathia pigmentosa reticularis hypohidotica...
    198 KB (17,965 words) - 14:19, 22 August 2024
  • Thumbnail for Naegeli–Franceschetti–Jadassohn syndrome
    fingerprint lines on the fingers. Naegeli syndrome is similar to dermatopathia pigmentosa reticularis, both of which are caused by a specific defect in the keratin...
    5 KB (447 words) - 15:04, 27 October 2023
  • Registrar, the former name of the UK Information Commissioner Dermatopathia pigmentosa reticularis, a congenital disorder Device pixel ratio, a measure of the...
    1 KB (213 words) - 22:44, 21 August 2024
  • cancer treatments such as radiation and alkylating agents Dermatopathia pigmentosa reticularis: genetic autosomal dominant condition Focal: Alopecia areata:...
    16 KB (1,792 words) - 17:40, 3 July 2024
  • Dermatoleukodystrophy Dermatomyositis Dermatoosteolysis, Kirghizian type Dermatopathia pigmentosa reticularis Dermatophytids Dermatophytosis Dermochondrocorneal dystrophy...
    13 KB (1,155 words) - 22:52, 28 April 2024
  • Thumbnail for Fingerprint
    People with Naegeli–Franceschetti–Jadassohn syndrome and dermatopathia pigmentosa reticularis, which are both forms of ectodermal dysplasia, also have...
    112 KB (12,062 words) - 03:16, 11 August 2024
  • Thumbnail for Keratin 14
    keratins are associated with epidermolysis bullosa simplex and dermatopathia pigmentosa reticularis, both of which are autosomal dominant mutations. 34βE12 (keratin...
    10 KB (1,175 words) - 17:23, 14 August 2024
  • Thumbnail for Dermatoglyphics
    (October 2006). "Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations...
    15 KB (1,681 words) - 23:18, 3 December 2023
  • Thumbnail for Gerodermia osteodysplastica
    fragility syndrome Ectodermal dysplasia Naegeli syndrome/Dermatopathia pigmentosa reticularis Hay–Wells syndrome Hypohidrotic ectodermal dysplasia Focal...
    14 KB (1,449 words) - 07:32, 22 July 2024
  • bullosa simplex Naegeli–Franceschetti–Jadassohn syndrome Dermatopathia pigmentosa reticularis Olmsted syndrome 15 16 Pachyonychia congenita type I 17 Pachyonychia...
    3 KB (161 words) - 16:22, 28 March 2023
  • bullosa simplex Naegeli–Franceschetti–Jadassohn syndrome Dermatopathia pigmentosa reticularis Olmsted syndrome KRT16 Pachyonychia congenita type I KRT17...
    12 KB (108 words) - 02:46, 17 September 2022
  • type III; 125500; DSPP Denys–Drash syndrome; 194080; WT1 Dermatopathia pigmentosa reticularis; 125595; KRT14 Desbuquois dysplasia; 251450; CANT1 Desmoid...
    234 KB (18,877 words) - 15:43, 9 May 2024