 Polydactyly
"Polydactyly" 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.
A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.
| Descriptor ID |
D017689
|
| MeSH Number(s) |
C05.660.585.600 C16.131.621.585.600
|
| Concept/Terms |
Polydactyly- Polydactyly
- Polydactylies
- Polydactylia
- Polydactylias
- Polydactylism
- Polydactylisms
- Hyperdactyly
- Hyperdactylies
|
Below are MeSH descriptors whose meaning is more general than "Polydactyly".
Below are MeSH descriptors whose meaning is more specific than "Polydactyly".
This graph shows the total number of publications written about "Polydactyly" by people in this website by year, and whether "Polydactyly" 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 |
|---|
| 1999 | 0 | 1 | 1 | | 2007 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Polydactyly" by people in Profiles.
-
Ullah I, Kakar N, Schrauwen I, Hussain S, Chakchouk I, Liaqat K, Acharya A, Wasif N, Santos-Cortez RLP, Khan S, Aziz A, Lee K, Couthouis J, Horn D, Kragesteen BK, Spielmann M, Thiele H, Nickerson DA, Bamshad MJ, Gitler AD, Ahmad J, Ansar M, Borck G, Ahmad W, Leal SM. Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly. Hum Genet. 2019 Jun; 138(6):593-600.
-
Schrauwen I, Giese AP, Aziz A, Lafont DT, Chakchouk I, Santos-Cortez RLP, Lee K, Acharya A, Khan FS, Ullah A, Nickerson DA, Bamshad MJ, Ali G, Riazuddin S, Ansar M, Ahmad W, Ahmed ZM, Leal SM. FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. J Bone Miner Res. 2019 02; 34(2):375-386.
-
Chang R, Petersen JR, Niswander LA, Liu A. A hypomorphic allele reveals an important role of inturned in mouse skeletal development. Dev Dyn. 2015 Jun; 244(6):736-47.
-
Lueth ET, Wood KE. McKusick Kaufman syndrome, complications arising at puberty. J Pediatr Adolesc Gynecol. 2014 Dec; 27(6):e125-6.
-
Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, Pearson CG, Kai M, Hartley J, Johnson C, Irving M, Elcioglu N, Winey M, Tada M, Scambler PJ. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy. Nat Genet. 2007 Jun; 39(6):727-9.
-
Rakheja D, Cimo ML, Ramus RM, Rogers BB, Bennett MJ, Boyer PJ, Galindo RL. Hydrolethalus syndrome, in contrast to Smith-Lemli-Opitz syndrome, is not due to a defect in post-squalene cholesterol biosynthesis: a case report. Am J Med Genet A. 2004 Aug 30; 129A(2):212-3.
-
Huang T, Elias ER, Mulliken JB, Kirse DJ, Holmes LB. A new syndrome: heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs. Genet Med. 1999 Mar-Apr; 1(3):104-8.
-
Hobbins JC, Jones OW, Gottesfeld S, Persutte W. Transvaginal ultrasonography and transabdominal embryoscopy in the first-trimester diagnosis of Smith-Lemli-Opitz syndrome, type II. Am J Obstet Gynecol. 1994 Aug; 171(2):546-9.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|