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Case Report: Alpha6 Integrin Disorder Presenting in Childhood with Nail Dysplasia and Onycholysis But No History of Fragile or Bullous Skin Changes.

Autor: Zalesny AN; OU Health Pediatric Specialties Clinic, Oklahoma Children's Hospital, Oklahoma City, Oklahoma, United States., Gunter S; OU Health Pediatric Specialties Clinic, Oklahoma Children's Hospital, Oklahoma City, Oklahoma, United States., Williams CA; Division of Genetics and Metabolism, Department of Pediatrics, University of Florida College of Medicine, Gainesville, Florida, United States.

Publikováno v: Global medical genetics [Glob Med Genet] 2024 Oct 16; Vol. 11 (4), pp. 344-348. Date of Electronic Publication: 2024 Oct 16 (Print Publication: 2024).

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First Report of a Known Pathogenic Variant in the FZD6 Gene, in an Iranian Family with Recessive Nail Dysplasia: A Case Report

Autor: Mirsajjad MOUSAVI-ASL GERMEH CHESHMEH, Ali NAJIZADEH, Saied HOSSEINI-ASL, Hooshang ZAIMKOHAN, Roshanak JAZAYERI

Publikováno v: Iranian Journal of Public Health, Vol 48, Iss 7 (2019)

Congenital Nail abnormalities are rare ectodermal defects. Autosomal recessive nail dysplasia is much rarer. Recently it has been recognized as a condition resulting in nail dystrophy in the absence of other cutaneous or extracutaneous disorders. Few

Externí odkaz: https://doaj.org/article/0c37025d97fa4d799bc0ac591be99f86

WITHDRAWN: Case Report: Alpha6 integrin disorder presenting in childhood with nail dysplasia and onycholysis but no history of fragile or bullous skin changes

Autor: Zalesny, Alayna N., Gunter, Sara, Williams, Charles A.

Publikováno v: In Global Medical Genetics