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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1985 1
1988 1
1992 1
2002 1
2003 1
2007 1
2008 1
2011 1
2013 1
2018 1
2021 2
2022 2
2023 1
2024 0

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15 results

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Page 1
A review of polydactyly and its inheritance: Connecting the dots.
Bubshait DK. Bubshait DK. Medicine (Baltimore). 2022 Dec 16;101(50):e32060. doi: 10.1097/MD.0000000000032060. Medicine (Baltimore). 2022. PMID: 36550802 Free PMC article. Review.
The phenotypic and genetic variability of polydactyly makes its etiology difficult to understand. Pre-axial polydactyly, central polydactyly (axial), and postaxial polydactyly are all examples of non-syndromic polydactyly (ulnar). ...PAP …
The phenotypic and genetic variability of polydactyly makes its etiology difficult to understand. Pre-axial polydactyly, centr …
Lower extremity postaxial polydactyly: Current literature status and future avenues.
Chocron Y, Kazan R, Abi-Rafeh J, Lessard A, Thibaudeau S. Chocron Y, et al. J Plast Reconstr Aesthet Surg. 2021 Nov;74(11):2977-2992. doi: 10.1016/j.bjps.2021.03.094. Epub 2021 Apr 18. J Plast Reconstr Aesthet Surg. 2021. PMID: 33992559 Review.
BACKGROUND: Despite lower extremity polydactyly (LEP) representing the most common congenital foot anomaly with functional and psychosocial implications, the literature is devoid of comprehensive, synthesizing reviews. The purpose of the current review is to identif …
BACKGROUND: Despite lower extremity polydactyly (LEP) representing the most common congenital foot anomaly with functional and …
Update of surgical treatment of polydactyly.
Tawfeeq Y, Hendry JM, Wood KS. Tawfeeq Y, et al. Curr Opin Pediatr. 2023 Feb 1;35(1):124-130. doi: 10.1097/MOP.0000000000001204. Epub 2022 Nov 22. Curr Opin Pediatr. 2023. PMID: 36412268 Review.
PURPOSE OF REVIEW: Polydactyly presents with variable extent of duplication and may involve preaxial/radial (hand)/medial (foot), postaxial/ulnar (hand)/lateral (foot) or central duplication. ...On-top plasty is an option that may be beneficial in 'une …
PURPOSE OF REVIEW: Polydactyly presents with variable extent of duplication and may involve preaxial/radial (hand)/medial (foot …
Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype Correlations.
Florea L, Caba L, Gorduza EV. Florea L, et al. Genes (Basel). 2021 Aug 29;12(9):1353. doi: 10.3390/genes12091353. Genes (Basel). 2021. PMID: 34573333 Free PMC article. Review.
The main clinical features are retinal cone-rod dystrophy, central obesity, postaxial polydactyly, cognitive impairment, hypogonadism and genitourinary abnormalities, and kidney disease. ...
The main clinical features are retinal cone-rod dystrophy, central obesity, postaxial polydactyly, cognitive impairment, hypog …
Polydactyly of the foot. Literature review and case presentations.
Galois L, Mainard D, Delagoutte JP. Galois L, et al. Acta Orthop Belg. 2002 Oct;68(4):376-80. Acta Orthop Belg. 2002. PMID: 12415940 Review.
Polydactyly is a fairly common congenital condition of the foot and is characterized literally by supernumerary toes (digit or metatarsal). ...Polydactyly is generally classified into three major groups: medial ray (preaxial), central ray and lateral ray ( …
Polydactyly is a fairly common congenital condition of the foot and is characterized literally by supernumerary toes (digit or …
Supernumerary and absent limbs and digits of the lower limb: a review of the literature.
Klaassen Z, Shoja MM, Tubbs RS, Loukas M. Klaassen Z, et al. Clin Anat. 2011 Jul;24(5):570-5. doi: 10.1002/ca.21102. Epub 2011 Jan 3. Clin Anat. 2011. PMID: 21647959 Review.
In 19th century Europe, a number of unique anomalies were reported, as well as evidence of foot amputations occurring in ancient Peruvian culture. Embryologically, the limbs develop early, with the lower limb being recognizable for the first time at stage 13 of development …
In 19th century Europe, a number of unique anomalies were reported, as well as evidence of foot amputations occurring in ancient Peru …
Meckel syndrome: genetics, perinatal findings, and differential diagnosis.
Chen CP. Chen CP. Taiwan J Obstet Gynecol. 2007 Mar;46(1):9-14. doi: 10.1016/S1028-4559(08)60100-X. Taiwan J Obstet Gynecol. 2007. PMID: 17389183 Free article. Review.
Pregnancies with MKS fetuses may be associated with an elevated maternal serum alpha-fetoprotein level and an abnormal screening result in the second-trimester maternal serum screening test. The classic MKS triad of occipital encephalocele, postaxial polydactyly, an …
Pregnancies with MKS fetuses may be associated with an elevated maternal serum alpha-fetoprotein level and an abnormal screening result in t …
Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb-polysyndactyly syndrome in a Chinese family and review of the literature.
Dai L, Guo H, Meng H, Zhang K, Hu H, Yao H, Bai Y. Dai L, et al. Eur J Pediatr. 2013 Nov;172(11):1467-73. doi: 10.1007/s00431-013-2071-y. Epub 2013 Jun 22. Eur J Pediatr. 2013. PMID: 23793141 Review.
Syndactyly type IV (SD4) is inherited in an autosomal dominant fashion and characterized by complete cutaneous syndactyly of all fingers accompanied with polydactyly. Triphalangeal thumb-polysyndactyly syndrome (TPTPS) consists of a triphalangeal thumb, polydactyly, …
Syndactyly type IV (SD4) is inherited in an autosomal dominant fashion and characterized by complete cutaneous syndactyly of all fingers acc …
Laurin-Sandrow syndrome: review and redefinition.
Mariño-Enríquez A, Lapunzina P, Omeñaca F, Morales C, Rodríguez JI. Mariño-Enríquez A, et al. Am J Med Genet A. 2008 Oct 1;146A(19):2557-65. doi: 10.1002/ajmg.a.32393. Am J Med Genet A. 2008. PMID: 18792985 Review.
She had hypertelorism, flat nose with grooved collumella, "V" shaped mouth with thin lips, 7 well-recognized and fused digits and 1 additional postaxial bilateral appendix on each hand. The right and left feet had 12 and 11 toes, respectively, the 4 external ones were reco …
She had hypertelorism, flat nose with grooved collumella, "V" shaped mouth with thin lips, 7 well-recognized and fused digits and 1 addition …
Limb anomalies in chromosomal aberrations.
Pfeiffer RA, Santelmann R. Pfeiffer RA, et al. Birth Defects Orig Artic Ser. 1977;13(1):319-37. Birth Defects Orig Artic Ser. 1977. PMID: 322750 Review.
Nothing has to be added to the teratologic series published by Muller [58] and, more recently, Willert and Henkel [109], but the distribution of the various manifestations may diverge. Asymmetry in 4q- (4r) is noteworthy. Postaxial polydactyly which is noted in tris …
Nothing has to be added to the teratologic series published by Muller [58] and, more recently, Willert and Henkel [109], but the distributio …
15 results