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Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz.

作者信息

Stieler Karola Maria, Bartzela Theodosia, Finke Christian, Blume-Peytavi Ulrike, Fischer Judith

机构信息

Department of Dermatology and Allergy, Charité, Universitätsmedizin Berlin, DE-10117 Berlin, Germany. E-mail:

出版信息

Acta Derm Venereol. 2020 Jul 28;100(14):adv00223. doi: 10.2340/00015555-3592.

DOI:10.2340/00015555-3592

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9199920/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c62/9199920/bdac134bda8a/ActaDV-100-14-5841-g002.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c62/9199920/050ce435a881/ActaDV-100-14-5841-g001.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c62/9199920/bdac134bda8a/ActaDV-100-14-5841-g002.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c62/9199920/050ce435a881/ActaDV-100-14-5841-g001.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c62/9199920/bdac134bda8a/ActaDV-100-14-5841-g002.jpg

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[3]

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[8]

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[9]

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[10]

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本文引用的文献

[1]

Short anagen syndrome: Case series and literature review.

Pediatr Dermatol. 2018-5

[2]

[WNT 10A-mutations as explanation for tooth agenesis].

Ned Tijdschr Tandheelkd. 2014-11

[3]

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Genet Med. 2015-5

[4]

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

Mol Genet Genomic Med. 2015-1

[5]

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

Br J Dermatol. 2014-10-15

[6]

WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.

Am J Med Genet A. 2014-2

[7]

Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

Clin Genet. 2011-1

[8]

Short anagen syndrome.

Pediatr Dermatol. 2011

[9]

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Am J Hum Genet. 2009-7

[10]

Trichodental dysplasia: a rare syndrome with distinct dental findings.

Pediatr Dent. 2006

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