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The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review.
Anbouba GM, Carmany EP, Natoli JL. Anbouba GM, et al. Am J Med Genet A. 2020 Apr;182(4):831-841. doi: 10.1002/ajmg.a.61493. Epub 2020 Jan 25. Am J Med Genet A. 2020. PMID: 31981414
The objective of this study was to review the published literature on X-linked hypohidrotic ectodermal dysplasia (XLHED) for the prevalence and characteristics of three features of XLHED: hypodontia, hypohidrosis, and hypotrichosis. A systematic search of English-language …
The objective of this study was to review the published literature on X-linked hypohidrotic ectodermal dysplasia (XLHED) for the prevalence …
Systematic review of oral and craniofacial findings in patients with Fabry disease or Pompe disease.
Benz K, Hahn P, Hanisch M, Lücke K, Lücke T, Jackowski J. Benz K, et al. Br J Oral Maxillofac Surg. 2019 Nov;57(9):831-838. doi: 10.1016/j.bjoms.2019.07.018. Epub 2019 Aug 9. Br J Oral Maxillofac Surg. 2019. PMID: 31405600
Common clinical signs of Fabry disease include hyposalivation, hypohidrosis, and xerophthalmia, and a generally reduced physical resilience was apparent in patients with Pompe disease. ...
Common clinical signs of Fabry disease include hyposalivation, hypohidrosis, and xerophthalmia, and a generally reduced physical resi …