Keratinocytic epidermal nevi associated with localized fibro‐osseous lesions without hypophosphatemia-Reference-Cited by-同舟云学术

Keratinocytic epidermal nevi associated with localized fibro‐osseous lesions without hypophosphatemia

Published:2020-07-14 Issue:5 Volume:37 Page:890-895
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Mestach Lien¹,Polubothu Satyamaanasa²³^ORCID,Calder Alistair⁴,Denayer Ellen⁵,Gholam Karolina³,Legius Eric⁵⁶,Levtchenko Elena⁷⁸,Van Laethem An¹,Brems Hilde⁵⁶,Kinsler Veronica A.²³,Morren Marie‐Anne¹^ORCID

Affiliation:

1. Department of Dermatology University Hospitals of Leuven Leuven Belgium

2. Genetics and Genomic Medicine UCL GOS Institute of Child Health London UK

3. Paediatric Dermatology Great Ormond Street Hospital for Children NHS Foundation Trust London UK

4. Paediatric Radiology Great Ormond Street Hospital for Children NHS Foundation Trust London UK

5. Center for Human Genetics University Hospital Leuven Leuven Belgium

6. Department of Human Genetics KU Leuven ‐ University of Leuven Leuven Belgium

7. Pediatric Nephrology University Hospitals of Leuven Leuven Belgium

8. Department of Development and Regeneration KU Leuven Leuven Belgium

Funder

Wellcome

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14254

Reference14 articles.

1. Keratinocytic epidermal nevi are associated with mosaicRASmutations

2. Phacomatosis Pigmentokeratotica Is Caused by a Postzygotic HRAS Mutation in a Multipotent Progenitor Cell

3. Postzygotic BRAF p.Lys601Asn Mutation in Phacomatosis Pigmentokeratotica with Woolly Hair Nevus and Focal Cortical Dysplasia

4. Male-to-male transmission of Costello syndrome: G12SHRASgermline mutation inherited from a father with somatic mosaicism

5. Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathy

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1. Mosaic RASopathies concept: different skin lesions, same systemic manifestations?;Journal of Medical Genetics;2024-01-30

2. Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation;Frontiers in Genetics;2023-08-10

4. Epidermal Nevus Syndromes;Neurocutaneous Disorders;2022

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