Nails, Malformed
"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
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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.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1999 | 1 | 0 | 1 | 2001 | 1 | 0 | 1 | 2005 | 1 | 0 | 1 | 2007 | 1 | 0 | 1 | 2017 | 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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Khan S, Ansar M, Khan AK, Shah K, Muhammad N, Shahzad S, Nickerson DA, Bamshad MJ, Santos-Cortez RLP, Leal SM, Ahmad W. A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family. Br J Dermatol. 2018 02; 178(2):556-558.
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Shah K, Ferrara TM, Jan A, Umair M, Khan S, Ahmad W, Spritz RA. Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbing. Br J Dermatol. 2017 08; 177(2):546-548.
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Ishii Y, Wajid M, Bazzi H, Fantauzzo KA, Barber AG, Blaydon DC, Nam JS, Yoon JK, Kelsell DP, Christiano AM. Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia. J Invest Dermatol. 2008 Apr; 128(4):867-70.
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Chen J, Roop DR. Mouse models in preclinical studies for pachyonychia congenita. J Investig Dermatol Symp Proc. 2005 Oct; 10(1):37-46.
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Camidge DR, Cameron DA. Brachial plexopathy affecting the development of Beau's lines unilaterally. Lancet Oncol. 2001 Jun; 2(6):342.
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Lin MT, Levy ML, Bowden PE, Magro C, Baden L, Baden HP, Roop DR. Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot. Exp Dermatol. 1999 Apr; 8(2):115-9.
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Aswegan AL, Josephson KD, Mowbray R, Pauli RM, Spritz RA, Williams MS. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. Am J Med Genet. 1997 Nov 12; 72(4):462-7.
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Horner RL, Wiedel JD, Bralliar F. Involvement of the hand in epidermolysis bullosa. J Bone Joint Surg Am. 1971 Oct; 53(7):1347-56.
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