"Nails, Malformed" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Deformities in nail structure or appearance, including hypertrophy, splitting, clubbing, furrowing, etc. Genetic diseases such as PACHYONYCHIA CONGENITA can result in malformed nails.
Descriptor ID |
D009264
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MeSH Number(s) |
C23.300.820
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Concept/Terms |
Nails, Abnormal- Nails, Abnormal
- Abnormal Nail
- Abnormal Nails
- Nail, Abnormal
- Nail Abnormalities
- Abnormalities, Nail
- Abnormality, Nail
- Nail Abnormality
|
Below are MeSH descriptors whose meaning is more general than "Nails, Malformed".
Below are MeSH descriptors whose meaning is more specific than "Nails, Malformed".
This graph shows the total number of publications written about "Nails, Malformed" by people in this website by year, and whether "Nails, Malformed" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2013 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2015 | 2 | 2 | 4 |
2016 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nails, Malformed" by people in Profiles.
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Identification of a Novel PLCD1 Variant in a Danish Family with Hereditary Leukonychia. Skinmed. 2023; 21(1):44-46.
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An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction. Br J Dermatol. 2018 04; 178(4):e265-e267.
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Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3. J Invest Dermatol. 2017 05; 137(5):1176-1179.
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Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature. Clin Exp Dermatol. 2016 Dec; 41(8):884-889.
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Nails - more than just an ectodermal appendage: the genetics behind isolated nail disorders. Br J Dermatol. 2015 Oct; 173(4):886.
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'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes. Hum Genet. 2015 Oct; 134(10):1089-97.
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Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes. Am J Med Genet A. 2015 Nov; 167A(11):2555-62.
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A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31. PLoS One. 2015; 10(6):e0129811.
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Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome. Am J Med Genet C Semin Med Genet. 2014 Sep; 166C(3):290-301.
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The genetic basis of DOORS syndrome: an exome-sequencing study. Lancet Neurol. 2014 Jan; 13(1):44-58.