Anetoderma in a patient with terminal osseous dysplasia with pigmentary defects
Author:
Affiliation:
1. Carver College of Medicine; University of Iowa Hospitals and Clinics
2. Stead Family Department of Pediatrics; University of Iowa Hospitals and Clinics
3. Department of Dermatology; University of Iowa Hospitals and Clinics
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37176/fullpdf
Reference21 articles.
1. Terminal osseous dysplasia and pigmentary defects: Clinical characterization of a novel male lethal X-linked syndrome;Bacino;Am J Med Genet,2000
2. Terminal osseous dysplasia with pigmentary defects: Clinical description of a new family;Baroncini;Am J Med Genet A,2007
3. Recurring digital fibroma of infancy;Bloem;J Bone Joint Surg Br,1974
4. Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations;Breuning;Am J Med Genet,2000
5. Terminal osseous dysplasia with pigmentary defects (TODPD) due to a recurrent filamin A (FLNA) mutation;Brunetti-Pierri;Mol Gen Genomic Med,2014
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1. Terminal osseous dysplasia with pigmentary defects in a Chinese girl with the FLNA mutation: A case report and published work review;The Journal of Dermatology;2020-01-09
2. Anetodermas and Atrophodermas;Harper's Textbook of Pediatric Dermatology;2019-11-20
3. Microdeletion in Xq28 with a polymorphic inversion in a patient with FLNA-associated progressive lung disease;Respiratory Investigation;2019-07
4. Cutaneous Elastic Tissue Anomalies;The American Journal of Dermatopathology;2019-02
5. Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings;American Journal of Medical Genetics Part A;2018-12-18
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