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Quoted phrase not found in phrase index: "Polysyndactyly 4"
Page 1
Hypothesis: Symbrachydactyly.
Holmes LB, Nasri HZ. Holmes LB, et al. Am J Med Genet A. 2022 Nov;188(11):3236-3241. doi: 10.1002/ajmg.a.62941. Epub 2022 Sep 8. Am J Med Genet A. 2022. PMID: 36073773
The term symbrachydactyly has been used for the phenotype of two or three short fingers or toes, hypoplasia of the middle and distal phalanges and variable syndactyly of the affected digits. Some clinicians have extended this diagnosis to include other phenotypes, specific …
The term symbrachydactyly has been used for the phenotype of two or three short fingers or toes, hypoplasia of the middle and distal phalang …
Constriction band syndrome.
Visuthikosol V, Hompuem T. Visuthikosol V, et al. Ann Plast Surg. 1988 Nov;21(5):489-95. doi: 10.1097/00000637-198811000-00017. Ann Plast Surg. 1988. PMID: 3232940
Good results were achieved in 16 of 20 patients with constriction band alone and in 4 of 10 acrosyndactyly cases. No compromised circulation of the distal limb or total flap loss was encountered in this study. ...
Good results were achieved in 16 of 20 patients with constriction band alone and in 4 of 10 acrosyndactyly cases. No compromised circ …
Triploidy: Variation of Phenotype.
Toufaily MH, Roberts DJ, Westgate MN, Holmes LB. Toufaily MH, et al. Am J Clin Pathol. 2016 Jan;145(1):86-95. doi: 10.1093/ajcp/aqv012. Am J Clin Pathol. 2016. PMID: 26712875
The abnormalities identified by prenatal ultrasound included renal malformations, heart defects, hydrocephalus, holoprosencephaly, and myelomeningocele. At autopsy, syndactyly, usually between fingers 3 and 4, was identified in 37 (69%) of the fetuses. ...CONCLUSION …
The abnormalities identified by prenatal ultrasound included renal malformations, heart defects, hydrocephalus, holoprosencephaly, and myelo …
Progressive Postnatal Pansynostosis.
Rogers GF, Greene AK, Proctor MR, Mulliken JB, Goobie SM, Stoler JM. Rogers GF, et al. Cleft Palate Craniofac J. 2015 Nov;52(6):751-7. doi: 10.1597/14-092. Epub 2014 Oct 28. Cleft Palate Craniofac J. 2015. PMID: 25350344
With the exception of one patient with moderate turricephaly, all patients had a relatively normal head shape with cranial indices ranging from 0.72 to 0.93 (mean, 0.81). Patients were diagnosed at an average of 32.4 months; craniosynostosis was suspected based on declinin …
With the exception of one patient with moderate turricephaly, all patients had a relatively normal head shape with cranial indices ranging f …
The Greig cephalopolysyndactyly syndrome.
Biesecker LG. Biesecker LG. Orphanet J Rare Dis. 2008 Apr 24;3:10. doi: 10.1186/1750-1172-3-10. Orphanet J Rare Dis. 2008. PMID: 18435847 Free PMC article. Review.
The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. The polydactyly is most commonly preaxial of the feet and postaxial in the hands, with variable cutaneous syndactyly, but the limb findings vary significantly. ...Ante …
The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. The polydactyly is most commonly p …
Poland's syndrome.
Urschel HC Jr. Urschel HC Jr. Chest Surg Clin N Am. 2000 May;10(2):393-403, viii. Chest Surg Clin N Am. 2000. PMID: 10803341 Review.
Poland's syndrome is characterized by hypoplasia or absence of the breast or nipple, hypoplasia of subcutaneous tissue, absence of the costosternal portion of the pectoralis major muscle, absence of the pectoralis minor muscle, and absence of costal cartilages or ribs 2, 3, and …
Poland's syndrome is characterized by hypoplasia or absence of the breast or nipple, hypoplasia of subcutaneous tissue, absence of the costo …
Presentation and Treatment of Poland Anomaly.
Buckwalter V JA, Shah AS. Buckwalter V JA, et al. Hand (N Y). 2016 Dec;11(4):389-395. doi: 10.1177/1558944716647355. Epub 2016 Oct 10. Hand (N Y). 2016. PMID: 28149203 Free PMC article. Review.
Operative management of syndactyly in Poland anomaly is determined by the severity of hand involvement and the resulting anatomical dysfunction. Syndactyly reconstruction is recommended in all but the mildest cases because most patients with Poland anomaly have nota …
Operative management of syndactyly in Poland anomaly is determined by the severity of hand involvement and the resulting anatomical d …
Common Pediatric Congenital Conditions of the Hand.
Kozin SH, Zlotolow DA. Kozin SH, et al. Plast Reconstr Surg. 2015 Aug;136(2):241e-257e. doi: 10.1097/PRS.0000000000001499. Plast Reconstr Surg. 2015. PMID: 26218399 Review.
Accurately diagnose congenital differences that affect the hand. 2. Develop a surgical plan for syndactyly with regard to timing of intervention to prevent progressive deformity and principles to restore the commissure. 3. List the potential complications following polydac …
Accurately diagnose congenital differences that affect the hand. 2. Develop a surgical plan for syndactyly with regard to timing of i …
The newborn foot.
Gore AI, Spencer JP. Gore AI, et al. Am Fam Physician. 2004 Feb 15;69(4):865-72. Am Fam Physician. 2004. PMID: 14989573 Free article. Review.
Common newborn foot abnormalities include metatarsus adductus, clubfoot deformity, calcaneovalgus (flexible flatfoot), congenital vertical talus (rigid flatfoot), and multiple digital deformities-polydactyly, syndactyly, overlapping toes, and amniotic bands. Most treatment …
Common newborn foot abnormalities include metatarsus adductus, clubfoot deformity, calcaneovalgus (flexible flatfoot), congenital vertical t …
Familial Poland anomaly revisited.
Baban A, Torre M, Costanzo S, Gimelli S, Bianca S, Divizia MT, Sénès FM, Garavelli L, Rivieri F, Lerone M, Valle M, Ravazzolo R, Calevo MG. Baban A, et al. Am J Med Genet A. 2012 Jan;158A(1):140-9. doi: 10.1002/ajmg.a.34370. Epub 2011 Nov 22. Am J Med Genet A. 2012. PMID: 22110015 Review.
Group1: true familial PA (F-PA): pectoral muscle defects with familial recurrence: 8(4.2%). Group2: familial Poland-like anomaly families (F-PLA): PA index case and 1 relative(s) showing normal pectoral muscles but ULA and/or TA common in PA: 16(8.4%). Group3: spora …
Group1: true familial PA (F-PA): pectoral muscle defects with familial recurrence: 8(4.2%). Group2: familial Poland-like anomaly fami …
357 results