Inherited skin disorders presenting with poikiloderma-Reference-Cited by-同舟云学术

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Inherited skin disorders presenting with poikiloderma

Published:2021-03-19 Issue:11 Volume:60 Page:1343-1353
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Rayinda Tuntas¹^ORCID,Steensel Maurice²³⁴,Danarti Retno¹^ORCID

Affiliation:

1. Department of Dermatology and Venereology Faculty of Medicine, Public Health, and Nursing Universitas Gadjah Mada Yogyakarta Indonesia

2. Skin Research Institute of Singapore Agency for Science, Technology and Research (A*STAR) Singapore Singapore

3. Lee Kong Chian School of Medicine Nanyang Technological University Singapore Singapore

4. National Skin Center Singapore Singapore

Funder

Black Metropolis Research Consortium

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.15498

Reference50 articles.

1. Poikiloderma: differential diagnosis and treatment;Nazari S;Pigment Disord,2015

2. Dermoscopic findings of poikiloderma in dyskeratosis congenita

3. Acquired poikiloderma: Proposed classification and diagnostic approach

4. Rothmund-Thomson syndrome

5. Rothmund's Syndrome—Thomson's Syndrome

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A photo‐distributed rash and eczematous eruptions in two siblings—A diagnostic conundrum;Australasian Journal of Dermatology;2024-04-22

2. Chinese nontwin sisters suffer from poikiloderma with neutropenia harboring novel compound heterozygous USB1 gene mutations;The Journal of Dermatology;2023-03-20

3. Hereditary fibrosing poikiloderma ( POIKTMP syndrome) report of a new mutation and review of the literature;Pediatric Dermatology;2022-09-14

4. Case Report: Diverse phenotypes of congenital poikiloderma associated with FAM111B mutations in codon 628: A case report and literature review;Frontiers in Genetics;2022-08-25

5. Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder;Human Molecular Genetics;2022-01-06

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