<scp>Conradi‐Hünermann‐Happle</scp> syndrome: Clinical and trichoscopic findings-Reference-Cited by-同舟云学术

Conradi‐Hünermann‐Happle syndrome: Clinical and trichoscopic findings

Published:2022-10-20 Issue:2 Volume:40 Page:333-336
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatric Dermatology

Author:

del Río‐Martínez Christopher Jesús¹,de León‐Jiménez Beatriz¹,Ramos‐Gómez Laura Isabel¹,Martinez Rebeca²,Durán‐Mckinster Carola³,Tosti Antonella⁴,Vázquez‐Herrera Norma Elizabeth¹

Affiliation:

1. Tecnologico de Monterrey Escuela de Medicina y Ciencias de la Salud Monterrey Mexico

2. Department of Dermatology Beth Israel Deaconess Medical Center Boston Massachusetts USA

3. Department of Dermatology National Institute of Pediatrics Mexico

4. Department of Dermatology and Cutaneous Surgery University of Miami Miller School of Medicine Miami Florida USA

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.15159

Reference18 articles.

1. Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature

2. Chondrodysplasia Punctata (Conradi Disease)

3. GeneReviews®. Chondrodysplasia punctata 2 X‐linked. Updated January 9 2020. Accessed November 21 2021.https://www.ncbi.nlm.nih.gov/books/NBK55062/?report=classic

4. Het syndroom van Conradi‐Hünermann‐Happle [Conradi‐Hünermann‐Happle syndrome];Bukkems SF;Ned Tijdschr Geneeskd,2012

5. Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome)

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