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
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
syndrome) Dermatopathia pigmentosa reticularis (dermatopathia pigmentosa reticularis hyperkeratotica et mutilans, dermatopathia pigmentosa reticularis hypohidotica...
198 KB (17,965 words) - 14:19, 22 August 2024
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...
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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
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
keratins are associated with epidermolysis bullosa simplex and dermatopathia pigmentosa reticularis, both of which are autosomal dominant mutations. 34βE12 (keratin...
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(October 2006). "Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations...
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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...
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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