Vernix Caseosa–like Hyperkeratotic Plaques in a French Canadian Infant-Reference-Cited by-同舟云学术

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Vernix Caseosa–like Hyperkeratotic Plaques in a French Canadian Infant

Published:2018-01-01 Issue:1 Volume:19 Page:e64-e68
ISSN:1526-9906
Container-title:NeoReviews
language:en
Short-container-title:

Author:

Al-Musalhi Buthaina¹,Lovett Audrey²,Srolovitz Herbert²,Jahnsen Frode L.³,Schlipf Nina⁴,Fischer Judith⁴,Khnykin Denis³

Affiliation:

1. Pediatric Dermatology, Sultan Qaboos University Hospital, Muscat, Oman

2. McGill University, Montreal, Canada

3. Department of Pathology and Centre for Immune Regulation, Oslo University Hospital, Rikshospitalet and University of Oslo, Oslo, Norway

4. Institute for Human Genetics, University Medical Center Freiburg, Freiburg, Germany

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Link

https://publications.aap.org/neoreviews/article-pdf/19/1/e64/821634/neoreviews_01al-musalhi.pdf

Reference11 articles.

1. Ichthyosis prematurity syndrome: clinical evaluation of 17 families with a rare disorder of lipid metabolism;Khnykin;J Am Acad Dermatol,2012

2. Prenatal sonographic assessment and perinatal course of ichthyosis prematurity syndrome;Blaas;Ultrasound Obstet Gynecol,2012

3. Ichthyosis prematurity syndrome with separation of fetal membranes and neonatal asphyxia;Dereksson;BMJ Case Rep,2012

4. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009;Oji;J Am Acad Dermatol,2010

5. Ichthyosis prematurity syndrome: a well-defined congenital ichthyosis subtype;Bygum;J Am Acad Dermatol,2008

Cited by 1 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. Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 gene;International Journal of Dermatology;2020-12-15

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