Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from Turkey-Reference-Cited by-同舟云学术

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Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from Turkey

Published:2020-09-06 Issue:6 Volume:33 Page:
ISSN:1396-0296
Container-title:Dermatologic Therapy
language:en
Short-container-title:Dermatologic Therapy

Author:

İmren Işıl Göğem¹^ORCID,Tanacan Efsun²^ORCID,Ceylaner Serdar³,Sumer Gokce⁴,Eksioglu Meral⁵^ORCID

Affiliation:

1. Department of Dermatology, Faculty of Medicine Pamukkale University Denizli Turkey

2. Department of Dermatology Ufuk University Ankara Turkey

3. Department of Medical Genetics İntergen Genetic Diagnosis and Research Center Ankara Turkey

4. Department of Pediatrics University of Health Sciences Ankara Research and Training Hospital Ankara Turkey

5. Department of Dermatology University of Health Sciences Ankara Research and Training Hospital Ankara Turkey

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dth.14152

Reference5 articles.

1. Genotype-phenotype correlations with TGM1 : clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis

2. A case of self‐improving collodion ichthyosis in Vietnam

3. Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients

4. Acral self-healing collodion baby: report of a new clinical phenotype caused by a novelTGM1mutation

5. Self-Healing Collodion Baby: a Dynamic Phenotype Explained by a Particular Transglutaminase-1 Mutation

Cited by 2 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. Concerning Newborn Rashes and Developmental Abnormalities: Part II: Congenital Infections, Ichthyosis, Neurocutaneous Disorders, Vascular Malformations, and Midline Lesions;Pediatrics in Review;2023-08-01

2. Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family;Medicina;2023-01-02

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